TWI856017B - Light-emitting device, display device, electronic device, organic compound, and lighting device - Google Patents

Abstract

A multicolor light-emitting device having high luminous efficiency is provided. The light-emitting device contains a material serving as an energy donor, a fluorescent material, and a phosphorescent material in a light-emitting layer. The material serving as an energy donor has a function of converting triplet excitation energy into light emission. The molecular structure of the fluorescent material includes a luminophore and protecting groups, and five or more protecting groups are contained in one molecule of a guest material. Introduction of protecting groups into molecules inhibits triplet excitation energy transfer from the material serving as an energy donor to the light-emitting material by the Dexter mechanism. Each of the protecting groups is an alkyl group or a branched-chain alkyl group. In the light-emitting device, light emission is obtained from both the fluorescent material and the phosphorescent material.

Description

Light-emitting element, display device, electronic device, organic compound and lighting equipment

An embodiment of the present invention relates to a light-emitting element, an organic compound, or a display device, an electronic device, and a lighting device including the light-emitting element.

Note that an embodiment of the present invention is not limited to the above-mentioned technical fields. The technical field of an embodiment of the invention disclosed in this specification and the like is related to an object, a method, or a manufacturing method. In addition, an embodiment of the present invention is related to a process, a machine, a product, or a composition of matter. Therefore, more specifically, as examples of the technical field of an embodiment of the present invention disclosed in this specification, there can be cited semiconductor devices, display devices, liquid crystal display devices, light-emitting devices, lighting equipment, power storage devices, memory devices, and driving methods or manufacturing methods of these devices.

In recent years, research and development of light-emitting devices using electroluminescence (EL) have become increasingly intense. The basic structure of these light-emitting devices is a structure in which a layer containing a light-emitting substance (EL layer) is sandwiched between a pair of electrodes. By applying a voltage between the electrodes of the device, light from the light-emitting substance can be obtained.

Since the light-emitting element is a self-luminous light-emitting element, a display device using the light-emitting element has the following advantages: good visibility, no need for backlight, low power consumption, etc. Moreover, the display device also has the following advantages: it can be made thin and light, and has a fast response speed, etc.

When a light-emitting element (e.g., an organic EL element) is used in which an organic compound is used as a light-emitting substance and an EL layer containing the light-emitting organic compound is provided between a pair of electrodes, by applying a voltage between the pair of electrodes, electrons and holes are injected from the cathode and the anode into the light-emitting EL layer, respectively, so that a current flows. Then, the injected electrons and holes are recombined to make the light-emitting organic compound into an excited state, and light emission can be obtained.

There are two types of excited states formed by organic compounds: singlet excited state (S*) and triplet excited state (T*). The emission from the singlet excited state is called fluorescence, and the emission from the triplet excited state is called phosphorescence. In addition, in the light-emitting element, the statistical generation ratio of the singlet excited state and the triplet excited state is S*:T*=1:3. Therefore, the light-emitting efficiency of the light-emitting element using the compound that emits phosphorescence (phosphorescent material) is higher than that of the light-emitting element using the compound that emits fluorescence (fluorescent material). Therefore, in recent years, research and development of light-emitting elements using phosphorescent materials that can convert triplet excited energy into light emission has become increasingly hot.

Among light-emitting elements using phosphorescent materials, especially light-emitting elements emitting blue light, it is difficult to develop stable compounds with high triplet excitation energy levels, so they have not yet been put into practical use. For this reason, light-emitting elements using more stable fluorescent materials have been developed, and methods for improving the light-emitting efficiency of light-emitting elements using fluorescent materials (fluorescent light-emitting elements) have been sought.

As a material capable of converting part or all of triplet excitation energy into luminescence, in addition to phosphorescent materials, thermally activated delayed fluorescence (TADF) materials are known. In TADF materials, a singlet excited state is generated from a triplet excited state by antisystem crossing, and the singlet excited state is converted into luminescence.

In order to improve the light-emitting efficiency in a light-emitting element using a TADF material, it is important not only to efficiently generate a singlet excited state from a triplet excited state in the TADF material, but also to efficiently obtain light emission from the singlet excited state, that is, to obtain a high fluorescence quantum yield. However, it is difficult to design a light-emitting material that satisfies both of the above conditions.

In addition, a method has been proposed in which, in a light-emitting element including a heat-activated delayed fluorescent material and a fluorescent material, the singlet excitation energy of the heat-activated delayed fluorescent material is transferred to the fluorescent material, and luminescence is obtained from the fluorescent material (see Patent Document 1).

[Patent Document 1] Japanese Patent Application Publication No. 2014-45179

[Non-patent literature 1] Hiroki Noda et al., “SCIENCE ADVANCES”, 2018, vol. 4, no. 6, eaao6910

[Non-patent document 2] S. Wang et al., Angew. Chem., Int. Ed. 54, 13068 (2015).

Multicolor light-emitting elements, represented by white light-emitting elements, are expected to be used in displays and the like. As an element structure for obtaining a multicolor light-emitting element, a light-emitting element having a plurality of EL layers disposed with a charge generating layer interposed therebetween (also called a series element) can be cited. In a series element, materials that emit different colors of light can be used for different EL layers, so a series element is suitable for the manufacture of a multicolor light-emitting element. However, since a series element has many layers, there is a problem of a large number of manufacturing processes.

Therefore, a light-emitting element capable of obtaining a plurality of luminescent colors from a single EL layer is required. In order to obtain a plurality of luminescent colors, two or more guest materials are used for the luminescent layer, but from the viewpoint of reliability, it is necessary to develop a multicolor light-emitting element using fluorescent materials.

As described above, as a method for improving the efficiency of a light-emitting element using a fluorescent material, for example, the following method can be cited: converting the triplet exciton of the host material into a singlet exciton and then transferring the singlet excitation energy to the fluorescent material as the guest material. However, when a fluorescent material is used as a guest material in the light-emitting layer of a light-emitting element, the lowest triplet excitation energy level (T1 level) of the fluorescent material does not contribute to luminescence, but sometimes becomes a deactivation path of the triplet excitation energy. Therefore, it is difficult to achieve high efficiency of a light-emitting element using a fluorescent material.

Therefore, in order to improve the luminous efficiency and reliability of a light-emitting element using a fluorescent material, it is preferred that the triplet excitation energy in the light-emitting layer is efficiently converted into singlet excitation energy and efficiently transferred to the fluorescent material as singlet excitation energy. To this end, it is necessary to develop a method that efficiently generates a singlet excitation state of a guest material from a triplet excitation state of a host material, thereby further improving the luminous efficiency of the light-emitting element and improving reliability.

Therefore, an object of an embodiment of the present invention is to provide a light-emitting element capable of obtaining a plurality of light-emitting colors from an EL layer. An object of an embodiment of the present invention is to provide a light-emitting element with high light-emitting efficiency. In addition, an object of an embodiment of the present invention is to provide a light-emitting element with reduced power consumption. In addition, an object of an embodiment of the present invention is to provide a novel light-emitting element. In addition, an object of an embodiment of the present invention is to provide a novel light-emitting device. In addition, an object of an embodiment of the present invention is to provide a novel display device.

Note that the description of the above-mentioned purpose does not hinder the existence of other purposes. An embodiment of the present invention does not necessarily need to achieve all of the above-mentioned purposes. In addition, purposes other than the above-mentioned purposes can be known and derived from the description of the specification, etc.

As described above, it is necessary to develop a method that can efficiently convert triplet excitation energy into luminescence in a fluorescent light-emitting element. To this end, it is necessary to improve the energy transfer efficiency between materials used in the light-emitting layer. To this end, it is necessary to suppress the transfer of triplet excitation energy between energy donors and energy acceptors based on the Dexter mechanism. At the same time, it is necessary to develop a light-emitting element that can efficiently obtain multi-color luminescence.

Therefore, one embodiment of the present invention is a light-emitting element, which includes a light-emitting layer between a pair of electrodes. The light-emitting layer includes a first material having a function of converting triplet excitation energy into luminescence, a second material having a function of converting singlet excitation energy into luminescence, and a third material having a function of converting triplet excitation energy into luminescence. The second material includes a luminescent body and five or more protecting groups. The luminescent body is a fused aromatic ring or a fused heteroaromatic ring. The five or more protecting groups independently have any one of an alkyl group having a carbon number of 1 to 10, a substituted or unsubstituted cycloalkyl group having a carbon number of 3 to 10, and a trialkylsilyl group having a carbon number of 3 to 12. The lowest triplet excitation energy level (T1 level) of the first material is higher than the T1 level of the third material. The light-emitting element obtains luminescence from both the second material and the third material.

In the above structure, it is preferred that at least four of the five or more protecting groups are independently any one of an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms.

In addition, another embodiment of the present invention is a light-emitting element, which includes a light-emitting layer between a pair of electrodes. The light-emitting layer includes a first material having a function of converting triplet excitation energy into luminescence, a second material having a function of converting singlet excitation energy into luminescence, and a third material having a function of converting triplet excitation energy into luminescence. The second material includes a luminescent body and four protecting groups. The luminescent body is a fused aromatic ring or a fused heteroaromatic ring. The four protecting groups are not directly bonded to the fused aromatic ring or the fused heteroaromatic ring. The four protecting groups independently have any one of an alkyl group having a carbon number of 3 or more and 10 or less, a substituted or unsubstituted cycloalkyl group having a carbon number of 3 or more and 10 or less, and a trialkylsilyl group having a carbon number of 3 or more and 12 or less. The T1 energy level of the first material is higher than the T1 energy level of the third material. The light emitting element obtains light from both the second material and the third material.

In addition, another embodiment of the present invention is a light-emitting element, which includes a light-emitting layer between a pair of electrodes. The light-emitting layer includes a first material having a function of converting triplet excitation energy into luminescence and a second material having a function of converting singlet excitation energy into luminescence. The second material includes a luminescent body and two or more diarylamine groups. The luminescent body is a fused aromatic ring or a fused heteroaromatic ring. The fused aromatic ring or the fused heteroaromatic ring is bonded to two or more diarylamine groups, and the two or more diarylamine groups independently have at least one protecting group. The protecting groups independently have any one of an alkyl group having 3 or more and 10 or less carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 or more and 10 or less carbon atoms, and a trialkylsilyl group having 3 or more and 12 or less carbon atoms. The light emitting element obtains light from both the first material and the second material.

In addition, another embodiment of the present invention is a light-emitting element, which includes a light-emitting layer between a pair of electrodes. The light-emitting layer includes a first material having a function of converting triplet excitation energy into luminescence, a second material having a function of converting singlet excitation energy into luminescence, and a third material having a function of converting triplet excitation energy into luminescence. The second material includes a luminophore and two or more diarylamine groups. The luminophore is a fused aromatic ring or a fused heteroaromatic ring. The fused aromatic ring or the fused heteroaromatic ring is bonded to two or more diarylamine groups, and the two or more diarylamine groups each independently have at least two protecting groups. The protecting groups independently include any one of an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms. The T1 energy level of the first material is higher than the T1 energy level of the third material. The light-emitting element obtains light from both the second material and the third material.

In the above structure, the diarylamine group is preferably a diphenylamine group.

In the above structure, the alkyl group is preferably a branched alkyl group.

In addition, another embodiment of the present invention is a light-emitting element, which includes a light-emitting layer between a pair of electrodes. The light-emitting layer includes a first material having a function of converting triplet excitation energy into luminescence, a second material having a function of converting singlet excitation energy into luminescence, and a third material having a function of converting triplet excitation energy into luminescence. The second material includes a luminophore and a plurality of protecting groups. The luminophore is a fused aromatic ring or a fused heteroaromatic ring. At least one of the atoms constituting the plurality of protecting groups is located directly on one face of the fused aromatic ring or the fused heteroaromatic ring. At least one of the atoms constituting the plurality of protecting groups is located directly on another face of the fused aromatic ring or the fused heteroaromatic ring. The T1 energy level of the first material is higher than the T1 energy level of the third material. The light-emitting element obtains luminescence from both the second material and the third material.

In addition, another embodiment of the present invention is a light-emitting element, which includes a light-emitting layer between a pair of electrodes. The light-emitting layer includes a first material having a function of converting triplet excitation energy into luminescence, a second material having a function of converting singlet excitation energy into luminescence, and a third material having a function of converting triplet excitation energy into luminescence. The second material includes a luminescent body and two or more diphenylamine groups. The luminescent body is a fused aromatic ring or a fused heteroaromatic ring. The fused aromatic ring or the fused heteroaromatic ring is bonded to two or more diphenylamine groups, and the phenyl groups in the two or more diphenylamine groups have protecting groups at the 3-position and the 5-position, respectively and independently. The protecting groups independently include any one of an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms. The T1 energy level of the first material is higher than the T1 energy level of the third material. The light-emitting element obtains light from both the second material and the third material.

In the above structure, the alkyl group is preferably a branched alkyl group.

In addition, in the above structure, the branched alkyl group preferably contains quaternary carbon.

(chrysene)、聯伸三苯、稠四苯、芘、苝、香豆素、喹吖啶酮以及萘并雙苯并呋喃中的至少一個。 In the above structure, the condensed aromatic ring or condensed heteroaromatic ring preferably includes naphthalene, anthracene, fluorene,

At least one of chrysene, triphenylene, tetraphenylene, pyrene, perylene, coumarin, quinacridone and naphthodibenzofuran.

In addition, in the above structure, preferably, the first material comprises a first organic compound and a second organic compound, and the first organic compound and the second organic compound form an excited complex. More preferably, the first organic compound exhibits phosphorescence.

In addition, in the above structure, the peak wavelength of the emission spectrum of the first material is preferably closer to the short wavelength side than the peak wavelength of the emission spectrum of the second material.

In addition, in the above structure, the first material is preferably a compound exhibiting phosphorescence or delayed fluorescence.

In addition, in the above structure, the emission spectrum of the first material preferably overlaps with the absorption band on the longest wavelength side of the absorption spectrum of the second material.

In addition, in the above structure, the concentration of the second material in the light-emitting layer is preferably higher than the concentration of the third material.

In addition, in the above structure, the third material is preferably a compound exhibiting phosphorescence.

In addition, in the above structure, the peak wavelength of the emission spectrum of the second material is preferably closer to the short wavelength side than the peak wavelength of the emission spectrum of the third material.

In addition, another embodiment of the present invention is a display device including a light-emitting element of each of the above structures, and at least one of a color filter and a transistor. In addition, another embodiment of the present invention is an electronic device including the above display device, and at least one of a housing and a touch sensor. In addition, another embodiment of the present invention is a lighting device including a light-emitting element of each of the above structures, and at least one of a housing and a touch sensor. In addition, an embodiment of the present invention is a light-emitting device having not only a light-emitting element but also an electronic device having a light-emitting device within its scope. Therefore, the light-emitting device in this specification refers to an image display device or a light source (including a lighting device). In addition, the light-emitting device sometimes also includes the following modules: a display module in which a connector such as FPC (Flexible Printed Circuit) or TCP (Tape Carrier Package) is installed on the light-emitting element; a display module in which a printed circuit board is provided at the end of the TCP; or a display module in which an IC (integrated circuit) is directly mounted on the light-emitting element by COG (Chip On Glass).

According to an embodiment of the present invention, a light-emitting element capable of obtaining a plurality of light-emitting colors from an EL layer can be provided. According to an embodiment of the present invention, a light-emitting element with high light-emitting efficiency can be provided. In addition, according to an embodiment of the present invention, a light-emitting element with reduced power consumption can be provided. In addition, according to an embodiment of the present invention, a novel light-emitting element can be provided. In addition, according to an embodiment of the present invention, a novel light-emitting device can be provided. In addition, according to an embodiment of the present invention, a novel display device can be provided.

Note that the description of these effects does not hinder the existence of other effects. In addition, one embodiment of the present invention does not necessarily need to have all of the above effects. In addition, effects other than the above effects can be known and derived from the description of the specification, drawings, patent application scope, etc.

100‧‧‧EL layer

101‧‧‧Electrode

102‧‧‧Electrode

106‧‧‧Light-emitting unit

108‧‧‧Light-emitting unit

111‧‧‧Hole injection layer

112‧‧‧Hole transport layer

113‧‧‧Electron Transmission Layer

114‧‧‧Electron injection layer

115‧‧‧Charge generation layer

116‧‧‧Hole injection layer

117‧‧‧Hole transport layer

118‧‧‧Electronic transmission layer

119‧‧‧Electron injection layer

120‧‧‧Luminescent layer

130‧‧‧Luminescent layer

131‧‧‧Compound

132‧‧‧Compound

133‧‧‧Compound

135‧‧‧Compound

136‧‧‧Compound

150‧‧‧Light-emitting element

170‧‧‧Luminescent layer

250‧‧‧Light-emitting element

301‧‧‧Objective Materials

302‧‧‧Objective Materials

310‧‧‧Luminous body

320‧‧‧Protection Base

330‧‧‧Main material

601‧‧‧Source side drive circuit

602‧‧‧Pixel Department

603‧‧‧Gate-side drive circuit

604‧‧‧Sealing substrate

605‧‧‧Sealant

607‧‧‧Space

608‧‧‧Wiring

609‧‧‧FPC

610‧‧‧Component substrate

611‧‧‧TFT for switch

612‧‧‧TFT for current control

613‧‧‧Electrode

614‧‧‧Insular

616‧‧‧EL layer

617‧‧‧Electrode

618‧‧‧Light-emitting element

623‧‧‧n-channel TFT

624‧‧‧p-channel TFT

625‧‧‧Desiccant

900‧‧‧Portable Information Terminal

901‧‧‧External shell

902‧‧‧External shell

903‧‧‧Display Department

905‧‧‧Hinge

910‧‧‧Portable Information Terminal

911‧‧‧External shell

912‧‧‧Display Department

913‧‧‧Operation button

914‧‧‧External port

915‧‧‧Speaker

916‧‧‧Microphone

917‧‧‧Camera

920‧‧‧Camera

921‧‧‧External shell

922‧‧‧Display Department

923‧‧‧Operation button

924‧‧‧Shutter button

926‧‧‧Lens

1001‧‧‧Substrate

1002‧‧‧Base insulation film

1003‧‧‧Gate insulation film

1006‧‧‧Gate electrode

1007‧‧‧Gate electrode

1008‧‧‧Gate electrode

1020‧‧‧Interlayer insulation film

1021‧‧‧Interlayer insulation film

1022‧‧‧Electrode

1024B‧‧‧Electrode

1024G‧‧‧Electrode

1024R‧‧‧Electrode

1024W‧‧‧Electrode

1025B‧‧‧Lower electrode

1025G‧‧‧Lower electrode

1025R‧‧‧Lower electrode

1025W‧‧‧Lower electrode

1026‧‧‧Partition wall

1028‧‧‧EL layer

1029‧‧‧Electrode

1031‧‧‧Sealing substrate

1032‧‧‧Sealant

1033‧‧‧Base material

1034B‧‧‧Color layer

1034G‧‧‧Color layer

1034R‧‧‧Color layer

1035‧‧‧Black layer

1036‧‧‧Protective layer

1037‧‧‧Interlayer insulation film

1040‧‧‧Pixel part

1041‧‧‧Drive circuit department

1042‧‧‧Peripheral Department

2100‧‧‧Robot

2101‧‧‧Illuminance sensor

2102‧‧‧Microphone

2103‧‧‧Upper camera

2104‧‧‧Speaker

2105‧‧‧Display

2106‧‧‧Lower camera

2107‧‧‧Obstacle Sensor

2108‧‧‧Mobile mechanism

2110‧‧‧Computing Device

5000‧‧‧External shell

5001‧‧‧Display Department

5002‧‧‧Display unit

5003‧‧‧Speaker

5004‧‧‧LED light

5005‧‧‧Operation keys

5006‧‧‧Connection terminal

5007‧‧‧Sensor

5008‧‧‧Microphone

5012‧‧‧Support Department

5013‧‧‧Headphone

5100‧‧‧Sweeping robot

5101‧‧‧Display

5102‧‧‧Camera

5103‧‧‧Brush

5104‧‧‧Operation button

5120‧‧‧Garbage

5140‧‧‧Portable electronic devices

5150‧‧‧Portable Information Terminal

5151‧‧‧External shell

5152‧‧‧Display area

5153‧‧‧Bend

8501‧‧‧Lighting equipment

8502‧‧‧Lighting equipment

8503‧‧‧Lighting equipment

8504‧‧‧Lighting equipment

In the drawings: FIG. 1A and FIG. 1B are schematic cross-sectional views of a light-emitting layer of a light-emitting element of an embodiment of the present invention, and FIG. 1C is a view illustrating the energy level correlation of a light-emitting layer of a light-emitting device of an embodiment of the present invention; FIG. 2A is a schematic view of a known guest material, and FIG. 2B is a schematic view of a guest material used in a light-emitting element of an embodiment of the present invention; FIG. 3A is a structural formula of a guest material used in a light-emitting element of an embodiment of the present invention, and FIG. 3B is a ball-and-stick diagram of a guest material used in a light-emitting element of an embodiment of the present invention; FIG4A is a schematic cross-sectional view of a light-emitting layer of a light-emitting element of an embodiment of the present invention, and FIGS. 4B to 4D are diagrams illustrating the energy level correlation of the light-emitting layer of a light-emitting device of an embodiment of the present invention; FIG5A is a schematic cross-sectional view of a light-emitting layer of a light-emitting element of an embodiment of the present invention, and FIGS. 5B and 5C are diagrams illustrating the energy level correlation of the light-emitting layer of a light-emitting device of an embodiment of the present invention; FIG6 is a schematic cross-sectional view of a light-emitting element of an embodiment of the present invention; FIG7A is a top view of a display device of an embodiment of the present invention, and FIG7B is a top view of a display device of an embodiment of the present invention; 8A and 8B are schematic cross-sectional views of a display device according to an embodiment of the present invention; FIGS. 9A and 9B are schematic cross-sectional views of a display device according to an embodiment of the present invention; FIGS. 10A to 10D are three-dimensional views of a display module according to an embodiment of the present invention; FIGS. 11A to 11C are views of an electronic device according to an embodiment of the present invention; FIGS. 12A and 12B are three-dimensional views of a display device according to an embodiment of the present invention; FIG. 13 is a view of a lighting device according to an embodiment of the present invention; and FIG. 14 is a view of a display module according to an embodiment of the present invention. FIG14 is a graph illustrating the external quantum efficiency-brightness characteristics of the light-emitting element according to the embodiment; FIG15 is a graph illustrating the electroluminescence spectrum of the light-emitting element according to the embodiment; FIG16 is a graph illustrating the relationship between the electroluminescence spectrum of the light-emitting element according to the embodiment, the absorption spectrum of the compound, and the emission spectrum; FIG17 is a graph illustrating the external quantum efficiency-brightness characteristics of the light-emitting element according to the embodiment; FIG18 is a graph illustrating the electroluminescence spectrum of the light-emitting element according to the embodiment; FIG19 is a graph illustrating the chromaticity-brightness characteristics of the light-emitting element according to the embodiment; and FIG20 is a graph illustrating the reliability test of the light-emitting element according to the embodiment. FIG21 is a diagram illustrating the electroluminescence spectrum of the light-emitting element before and after the reliability test according to the embodiment; FIG22A and FIG22B are diagrams illustrating the NMR spectrum of the compound according to the reference example; FIG23 is a diagram illustrating the NMR spectrum of the compound according to the reference example; FIG24A and FIG24B are diagrams illustrating the NMR spectrum of the compound according to the reference example; FIG25 is a diagram illustrating the NMR spectrum of the compound according to the reference example; FIG26 is a diagram illustrating the external quantum efficiency-brightness characteristics of the light-emitting element according to the embodiment; FIG27 is a diagram illustrating the electroluminescence spectrum of the light-emitting element according to the embodiment; Figure 28 is a graph illustrating the external quantum efficiency-brightness characteristics of the light-emitting element according to the embodiment; Figure 29 is a graph illustrating the electroluminescence spectrum of the light-emitting element according to the embodiment; Figures 30A and 30B are graphs illustrating the NMR spectrum of the compound according to the reference example; Figure 31 is a graph illustrating the NMR spectrum of the compound according to the reference example.

The selected diagrams of the present invention are FIG. 2A and FIG. 2B .

The following is a detailed description of the embodiments of the present invention with reference to the drawings. Note that the present invention is not limited to the following description, and its methods and details can be transformed into various forms without departing from the spirit and scope of the present invention. Therefore, the present invention should not be interpreted as being limited to the contents described in the embodiments shown below.

In addition, for easy understanding, the position, size, range, etc. of each structure shown in the drawings and the like sometimes do not represent its actual position, size, range, etc. Therefore, the disclosed invention is not necessarily limited to the position, size, range, etc. disclosed in the drawings and the like.

In addition, in this specification, for easy understanding, ordinal numbers such as first and second are added, but they do not sometimes indicate the process order or stacking order. Therefore, for example, "first" can be appropriately replaced with "second" or "third" for description. In addition, the ordinal numbers recorded in this specification and the like are sometimes inconsistent with the ordinal numbers used to specify an embodiment of the present invention.

Note that in this specification and the like, when describing the structure of the invention using drawings, symbols representing the same parts may be used in common in different drawings.

In addition, in this specification, "film" and "layer" may be interchanged. For example, "conductive layer" may be replaced by "conductive film". Also, "insulating film" may be replaced by "insulating layer".

In addition, in this specification, etc., a singlet excited state (S ^* ) refers to a singlet state having excitation energy. In addition, an S1 energy level is the lowest energy level of the singlet excited energy level, and it refers to the excitation energy level of the lowest singlet excited state (S1 state). In addition, a triplet excited state (T ^* ) refers to a triplet state having excitation energy. In addition, a T1 energy level is the lowest energy level of the triplet excited energy level, and it refers to the excitation energy level of the lowest triplet excited state (T1 state). In addition, in this specification, etc., although sometimes simply "singlet excited state" and "singlet excited energy level" are described, sometimes they represent the S1 state and the S1 energy level, respectively. In addition, even when "triplet excited state" and "triplet excited energy level" are described, they may represent the T1 state and the T1 energy level, respectively.

In this specification, a fluorescent material refers to a compound that emits light in the visible light region when returning from a singlet excited state to a ground state. A phosphorescent material refers to a compound that emits light in the visible light region at room temperature when returning from a triplet excited state to a ground state. In other words, a phosphorescent material refers to one of the compounds that can convert triplet excited energy into visible light.

Note that in this specification and the like, room temperature refers to a temperature within a range of 0° C. or higher and 40° C. or lower.

In addition, in this specification, etc., the blue wavelength region refers to a wavelength region greater than 400nm and less than 490nm, and blue luminescence has at least one emission spectrum peak in this wavelength region. In addition, the green wavelength region refers to a wavelength region greater than 490nm and less than 580nm, and green luminescence has at least one emission spectrum peak in this wavelength region. In addition, the red wavelength region refers to a wavelength region greater than 580nm and less than 680nm, and red luminescence has at least one emission spectrum peak in this wavelength region. In addition, even in the case where two emission spectra have emission spectrum peaks in the same wavelength region, when the peak wavelengths are different, the emission colors of the two emission spectra are sometimes regarded as different. Note that the emission spectrum peak is a maximum value, or includes a shoulder peak.

Implementation method 1

In this embodiment, a light emitting element according to an embodiment of the present invention is described with reference to FIG. 1A to FIG. 5C .

〈Structural example of light-emitting element〉

First, the structure of a light emitting element according to an embodiment of the present invention will be described with reference to FIGS. 1A to 1C .

FIG. 1A is a schematic cross-sectional view of a light emitting element 150 according to an embodiment of the present invention.

The light emitting element 150 includes a pair of electrodes (electrode 101 and electrode 102 ) and an EL layer 100 disposed between the pair of electrodes. The EL layer 100 includes at least a light emitting layer 130 .

In addition, the EL layer 100 shown in FIG. 1A includes functional layers such as a hole injection layer 111 , a hole transport layer 112 , an electron transport layer 118 , and an electron injection layer 119 in addition to the light-emitting layer 130 .

Note that although the present embodiment describes the electrode 101 of a pair of electrodes as an anode and the electrode 102 as a cathode, the structure of the light-emitting element 150 is not limited thereto. In other words, the electrode 101 may be used as a cathode and the electrode 102 may be used as an anode, and the order of the layers between the electrodes may be reversed. In other words, the hole injection layer 111, the hole transport layer 112, the light-emitting layer 130, the electron transport layer 118, and the electron injection layer 119 may be stacked in sequence from the anode side.

Note that the structure of the EL layer 100 is not limited to the structure shown in FIG. 1A , as long as it includes at least one selected from the hole injection layer 111, the hole transport layer 112, the electron transport layer 118, and the electron injection layer 119. Alternatively, the EL layer 100 may include a functional layer having the following functions: a functional layer capable of reducing the injection barrier of holes or electrons; a functional layer capable of improving the transport properties of holes or electrons; a functional layer capable of blocking the transport properties of holes or electrons; or a functional layer capable of suppressing the quenching phenomenon caused by the electrode, etc. The functional layer may be a single layer or a stack of multiple layers.

<Light-emitting mechanism of light-emitting element>

The light emitting mechanism of the light emitting layer 130 is described below.

In the light-emitting element 150 of one embodiment of the present invention, by applying a voltage between a pair of electrodes (electrode 101 and electrode 102), electrons and holes are injected from the cathode and anode into the EL layer 100, respectively, so that current flows. Among the excitons generated by the recombination of carriers (electrons and holes), the statistical probability of the ratio of singlet excitons to triplet excitons (hereinafter referred to as the exciton generation probability) is 1:3. Therefore, the ratio of generating singlet excitons is 25%, and the ratio of generating triplet excitons is 75%. Therefore, in order to improve the luminous efficiency of the light-emitting element, it is important to make the triplet exciton contribute to luminescence. Therefore, as the light-emitting layer 130, it is preferable to use a material having the function of converting triplet excitation energy into luminescence.

As a material having the function of converting triplet excitation energy into luminescence, a compound capable of emitting phosphorescence (hereinafter referred to as a phosphorescent material) can be cited. In this specification, etc., a phosphorescent material refers to a compound that emits phosphorescence but not fluorescence at any temperature in a temperature range of above low temperature (e.g., 77K) and below room temperature (i.e., above 77K and below 313K). The phosphorescent material preferably contains a metal element having a large spin-orbit interaction, specifically, preferably contains a transition metal element, particularly preferably contains a platinum group element (ruthenium (Ru), rhodium (Rh), palladium (Pd), niobium (Os), iridium (Ir) or platinum (Pt)), and particularly preferably contains iridium. Iridium is preferred because it increases the probability of the direct transition between the singlet ground state and the triplet excited state.

In addition, as a material having the function of converting triplet excitation energy into luminescence, TADF materials can be cited. TADF materials refer to materials that have a small difference between the S1 energy level and the T1 energy level and have the function of converting triplet excitation energy into singlet excitation energy by antisystem crossing. Therefore, it is possible to up-convert triplet excitation energy into singlet excitation energy (antisystem crossing) using tiny thermal energy and efficiently generate a singlet excited state. Exciplexes that form excited states with two substances have the function of TADF materials that convert triplet excitation energy into singlet excitation energy because the difference between the S1 energy level and the T1 energy level is extremely small.

As an indicator of the T1 energy level, the phosphorescence spectrum observed at a low temperature (e.g., 10 K) can be used. For TADF materials, it is preferred that a tangent line is drawn at the tail of the short-wavelength side of the fluorescence spectrum, and the energy of the wavelength of the extrapolated line is set to the S1 energy level, and a tangent line is drawn at the tail of the short-wavelength side of the phosphorescence spectrum, and the energy of the wavelength of the extrapolated line is set to the T1 energy level. At this time, the difference between S1 and T1 is less than 0.2 eV.

In addition, as a material having the function of converting triplet excitation energy into luminescence, a nanostructure of a transition metal compound having a calcium-titanium structure can be cited. A metal halide calcium-titanium nanostructure is particularly preferred. As the nanostructure, nanoparticles and nanorods are preferred.

FIG1B is a schematic cross-sectional view of a light-emitting layer 130 of a light-emitting element according to an embodiment of the present invention. In an embodiment of the present invention, the light-emitting layer 130 comprises compound 131, compound 132 and compound 136. Compound 131 has a function of converting triplet excitation energy into luminescence, compound 132 has a function of converting singlet excitation energy into luminescence, and compound 136 has a function of converting triplet excitation energy into luminescence. Since the stability of fluorescent materials is high, it is preferred to use fluorescent materials as compound 132 to obtain a light-emitting element with high reliability. In addition, since compound 131 has a function of converting triplet excitation energy into luminescence, in order to obtain a light-emitting element with high luminescence efficiency, it is preferred to generate carrier recombination in compound 131. Therefore, it is preferred that both the singlet excitation energy and triplet excitation energy of the excitons generated by the recombination of carriers in compound 131 are ultimately transferred to the singlet excited state of compound 132 and the excited state of compound 136 (triplet excited state of phosphorescent material, singlet excited state of TADF material), and compound 132 and compound 136 emit light. Here, in the light-emitting layer 130, compound 131 has the function of an energy donor, and compound 132 and compound 136 have the function of an energy acceptor. In FIG1C , the light-emitting layer 130 is a fluorescent light-emitting layer having compound 131 as a host material and compound 132 and compound 136 as guest materials. That is, in FIG1C , the host material is used as an energy donor, and the guest material is used as an energy acceptor. In addition, the light-emitting layer 130 can obtain light emission from the compound 132 and the compound 136 as guest materials.

〈Structural example 1 of the light-emitting layer〉

1C shows an example of the energy level correlation in the light-emitting layer of the light-emitting element according to one embodiment of the present invention. In this structural example, the case where the compound 131 uses a TADF material and the compound 136 uses a phosphorescent material is shown.

1C shows the energy level correlation of compound 131, compound 132, and compound 136 in the light-emitting layer 130. The symbols and signs in FIG1C are as follows.

‧Host(131): Compound 131

‧Fluorecent Guest (132): Compound 132

‧Phosphorecent Guest (136): Compound 136

_‧TC1 : T1 energy level of compound 131

‧S _C1 : S1 energy level of compound 131

_‧SFG : S1 energy level of compound 132

_‧TFG : T1 energy level of compound 132

‧T _PG : T1 energy level of compound 136

S_FG。明確而言，較佳的是，在化合物131的螢光光譜的短波長一側的尾處劃切線，將該外推線的波長的能量設定為S_C1，將化合物132的吸收光譜的吸收端的波長的能量設定為S_FG，此時滿足S_C1

S_FG。此外，由於化合物136是磷光材料，所以能夠接收化合物131所具有的單重激發能及三重激發能(圖1C的路徑A₃)。此時，較佳為S_C1

T_C1

T_PG。此外，可以將化合物136的吸收光譜的吸收端的波長的能量視為T_PG。此外，可以將化合物131的低溫(例如10K)下的發射光譜的短波長一側的發射端的波長能量視為T_C1。 Here, we focus on the triplet excitation energy of compound 131 generated by current excitation. Compound 131 has TADF characteristics. Therefore, compound 131 has the function of converting triplet excitation energy into singlet excitation energy by up-conversion (path _A1 in Figure 1C). The singlet excitation energy of compound 131 can be quickly transferred to compound 132 (path _A2 in Figure 1C). At this time, it is preferred to satisfy _SC1

Specifically, it is preferred that a tangent line be drawn at the tail of the short-wavelength side of the fluorescence spectrum of compound 131, the energy of the _wavelength of the extrapolated line be set as S _C1 , and the energy of the wavelength at the absorption end of the absorption spectrum of compound 132 be set as S _FG , and then S _C1 is satisfied.

In addition, since compound 136 is a phosphorescent material, it can receive the singlet excitation energy and triplet excitation energy of compound 131 (path A ₃ in FIG. _1C ). In this case, preferably S _C1

T _C1

T _PG . In addition, the energy of the wavelength at the absorption end of the absorption spectrum of compound 136 can be regarded as T _PG . In addition, the energy of the wavelength at the emission end on the short wavelength side of the emission spectrum of compound 131 at a low temperature (eg, 10 K) can be regarded as T _C1 .

The triplet excitation energy generated in compound 131 is transferred to the S1 energy level of compound 132 as the guest material via the above-mentioned paths _A1 and _A2 , and compound 132 emits light, thereby converting the triplet excitation energy into fluorescent light, thereby improving the light-emitting efficiency of the light-emitting element. In addition, since compound 136 can also convert the triplet excitation energy into light, when compound 132 and compound 136 exhibit different light-emitting colors, multi-color light emission can be efficiently obtained.

Here, in the light-emitting layer 130, the compound 131, the compound 132, and the mixture 136 are mixed together. Therefore, there is a possibility that the triplet excitation energy of the compound 131 is converted into the triplet excitation energy of the compound 132 in competition with the above-mentioned paths _A1 , _A2 , and _A3 (path _A4 in FIG. 1C). Since the compound 132 is a fluorescent material, the triplet excitation energy of the compound 132 does not contribute to luminescence. That is, when the energy transfer of the path _A4 occurs, the luminescence efficiency of the light-emitting element decreases. Note that, in reality, as the energy transfer path _A4 from _TC1 to _TFG , there may be a path that is not direct but is converted to _TFG by internal conversion once the energy is transferred to the triplet excited state higher than _TFG of the compound 132, but this process is omitted in the figure. The undesirable heat inactivation process in the following description of the invention, i.e., the inactivation process to _TFG, is the same.

T_PG時，化合物132所具有的單重激發能被轉換為螢光發光的過程與被轉移到T_PG的過程(圖1C的路徑A₅)競爭。也就是說，作為化合物136接收激發能的過程，存在路徑A₃及A₅。因此，為了以良好的比率獲得化合物132及化合物136的發光的兩者，較佳為發光層130中的化合物132的濃度高於化合物136的濃度。此外，較佳為發光層130中的化合物136的濃度較低，因為載子不容易在化合物136中再結合。 In addition, as shown in Figure 1C, when S _FG

When _TPG , the process in which the singlet excitation energy of compound 132 is converted into fluorescent luminescence competes with the process in which it is transferred to _TPG (path _A5 in FIG1C ). That is, as a process in which compound 136 receives excitation energy, there are paths _A3 and _A5 . Therefore, in order to obtain both luminescence of compound 132 and compound 136 at a good ratio, it is preferred that the concentration of compound 132 in the luminescent layer 130 is higher than the concentration of compound 136. In addition, it is preferred that the concentration of compound 136 in the luminescent layer 130 is lower because carriers are not easily recombined in compound 136.

In addition, there is a competition between the process in which the triplet excitation energy of compound 136 is converted into luminescence and the process in which the triplet excitation energy of compound 136 is converted into the triplet excitation energy of compound 132 (path _A6 in FIG1C ). Since compound 132 is a fluorescent material, the triplet excitation energy of compound 132 does not contribute to luminescence. That is, when the energy transfer of path _A6 occurs, the luminescence efficiency of the light-emitting element decreases.

In addition, the shorter the emission wavelength of the luminescence presented by the compound, the higher the energy at which the compound is excited. Therefore, in order to obtain good reliability of the light-emitting element, it is preferred to use a luminescent material with a high luminescence rate constant as a compound presenting short-wavelength luminescence, preferably a fluorescent material. In other words, it is preferred that the luminescence presented by compound 132 has a luminescence peak on the shorter wavelength side compared to the luminescence presented by compound 136.

As the energy transfer mechanism between molecules, the Förster mechanism (dipole-dipole interaction) and the Dexter mechanism (electron exchange interaction) are known. Since compound 132, which is an energy acceptor, is a fluorescent material, the Dexter mechanism occurs significantly in the energy transfer of paths _A4 and _A6 . Generally speaking, the Dexter mechanism occurs significantly when the distance between compound 131 and compound 136, which supply energy, and compound 132, which is an energy acceptor, is less than 1 nm. Therefore, in order to suppress paths _A4 and _A6 , it is important to make the distance between the energy donor and the energy acceptor long.

Since the direct transition from the singlet ground state to the triplet excited state in compound 132 is a forbidden transition, the energy transfer from the singlet excited energy level (S _C1 ) of compound 131 to the triplet excited energy level ( _TFG ) of compound 132 is unlikely to become the main energy transfer process and is therefore not shown.

Most of the _TFG in FIG1C is derived from the energy level of the luminescent body of the fluorescent compound. Therefore, in more detail, in order to suppress the paths _A4 and _A6 , it is important to lengthen the distance between the energy donor and the luminescent body included in the fluorescent compound that receives the energy. As a method for lengthening the distance between the energy donor and the luminescent body included in the fluorescent compound, generally, it is cited to reduce the concentration of the fluorescent compound in the mixed film of these compounds. However, when the concentration of the energy acceptor in the mixed film is reduced, in addition to the energy transfer based on the Dexter mechanism from the energy donor to the fluorescent compound, the energy transfer based on the Foster mechanism is also suppressed. At this time, because the path _A2 is based on the Foster mechanism, problems such as a reduction in the luminous efficiency of the light-emitting element or a reduction in reliability occur.

Therefore, the inventors of this case found that the reduction in the above-mentioned luminescence efficiency can be suppressed by using a fluorescent material having a protective group for increasing the distance between the fluorescent material and the energy donor as an energy acceptor. In addition, the inventors of this case found that by using the above-mentioned fluorescent material, both fluorescent luminescence and phosphorescent luminescence can be obtained from a luminescent layer in which the fluorescent material and the phosphorescent material are mixed.

〈Concept of fluorescent materials with protective groups〉

FIG2A is a schematic diagram showing a case where a fluorescent material without a protective group as a general fluorescent material is dispersed in a host material as a guest material, and FIG2B is a schematic diagram showing a case where a fluorescent material with a protective group used in a light-emitting element of an embodiment of the present invention is dispersed in a host material as a guest material. The host material can be referred to as an energy donor and the guest material can be referred to as an energy acceptor. Here, the protective group has a function of lengthening the distance between the luminescent body and the host material. In FIG2A , the guest material 301 has a luminescent body 310. The guest material 301 is used as an energy acceptor. On the other hand, in FIG2B , the guest material 302 includes a luminescent body 310 and a protective group 320. In FIG2A and FIG2B , the guest material 301 and the guest material 302 are surrounded by the host material 330. In FIG2A, because the distance between the luminescent body and the host material is short, energy transfer based on the Foster mechanism (path _A7 in FIG2A and FIG2B) and energy transfer based on the Dexter mechanism (path _A8 in FIG2A and FIG2B) may occur as energy transfer from the host material 330 to the guest material 301. When the energy transfer of triplet excitation energy from the host material to the guest material based on the Dexter mechanism occurs to generate a triplet excited state of the guest material, when the guest material is a fluorescent material, non-radiative deactivation of the triplet excitation energy occurs, which becomes one of the reasons for the decrease in the luminous efficiency of the light-emitting element.

On the other hand, in FIG. 2B , the guest material 302 has a protective group 320. Therefore, the distance between the luminescent body 310 and the host material 330 can be made long. Therefore, the energy transfer based on the Dexter mechanism (path A ₈ ) can be suppressed. Therefore, by using a fluorescent material having a protective group such as the guest material 302 for the luminescent layer 130 shown in FIGS. 1A to 1C , the paths A ₄ and A ₆ in FIG. 1C can be suppressed.

Here, in order to make the object material 302 emit light, the object material 302 needs to receive energy from the host material 330 based on the Foster mechanism because the Dexter mechanism is suppressed. That is, it is better to efficiently utilize the energy transfer based on the Foster mechanism while suppressing the energy transfer based on the Dexter mechanism. It is known that the energy transfer based on the Foster mechanism is also affected by the distance between the host material and the object material. Generally speaking, when the distance between the host material 330 and the object material 302 is less than 1nm, the Dexter mechanism is dominant, and when it is greater than 1nm and less than 10nm, the Foster mechanism is dominant. Generally speaking, when the distance between the host material 330 and the object material 302 is greater than 10nm, energy transfer is not easy to occur. Here, the distance between the host material 330 and the guest material 302 may be referred to as the distance between the host material 330 and the light-emitting body 310 .

Therefore, the protective base 320 preferably diffuses within a range of 1 nm to 10 nm from the luminescent body 310. More preferably, it diffuses within a range of 1 nm to 5 nm from the luminescent body 310. By adopting this structure, energy transfer based on the Dexter mechanism can be efficiently utilized while suppressing energy transfer based on the Foster mechanism from the host material 330 to the guest material 302. Therefore, a light-emitting element with high light-emitting efficiency can be manufactured.

In addition, in order to improve the energy transfer efficiency based on the Foster mechanism (increase the energy transfer speed), it is preferable to increase the concentration of the guest material 301 or the guest material 302 relative to the host material 330. However, generally, when the concentration of the guest material is increased, the energy transfer speed of the Dexter mechanism also becomes faster, which leads to a decrease in the luminescence efficiency. Therefore, it is difficult to increase the concentration of the guest material. There is a report on the following light-emitting element: in a fluorescent light-emitting element using a material having a function of converting triplet excitation energy into luminescence as a host material, the concentration of the guest material is as low as 1wt% or less.

On the other hand, in a light-emitting element of an embodiment of the present invention, a fluorescent material having a protective group as a light-emitting body is used for the light-emitting layer. As a result, the energy transfer based on the Dexter mechanism can be efficiently utilized while suppressing the energy transfer based on the Dexter mechanism, so the concentration of the fluorescent material as an energy acceptor can be increased. As a result, an originally contradictory phenomenon can be achieved, that is, the energy transfer rate based on the Foster mechanism can be increased while suppressing the energy transfer based on the Dexter mechanism. The concentration of the fluorescent material relative to the host material is preferably greater than 1wt% and less than 30wt%, more preferably greater than 5wt% and less than 20wt%, and further preferably greater than 5wt% and less than 15wt%. By adopting this structure, the energy transfer rate based on the Foster mechanism can be increased, so a light-emitting element with high luminous efficiency can be obtained. Furthermore, by using a material having the function of converting triplet excitation energy into luminescence as a main material, a fluorescent light-emitting element having a high luminescence efficiency equal to that of a phosphorescent light-emitting element can be manufactured. In addition, since the luminescence efficiency is improved by using a highly stable fluorescent material, a highly reliable light-emitting element can be manufactured. In addition, a phosphorescent material is also used in the light-emitting element of an embodiment of the present invention. Thus, both fluorescent luminescence and phosphorescent luminescence can be obtained with high luminescence efficiency.

In addition, in particular, the effect of the light-emitting element of one embodiment of the present invention is not only the effect of improving reliability caused by the use of highly stable fluorescent materials. The above-mentioned energy transfer often competes with the quenching process caused by the influence of deterioration or impurities. When the quenching rate constant of the quenching process increases with time, the luminescence ratio of the light-emitting element decreases. That is, the brightness of the light-emitting element deteriorates. However, as described above, in one embodiment of the present invention, while suppressing the energy transfer based on the Dexter mechanism, the energy transfer rate based on the Foster mechanism can be made higher than that of the known light-emitting element. Therefore, the influence brought about by the competition with the quenching process can be reduced, and the life of the element can be extended.

Here, the luminescent body refers to an atomic group (skeleton) that is the cause of luminescence in a fluorescent material. The luminescent body generally has a π bond, preferably includes an aromatic ring, and preferably has a fused aromatic ring or a fused heteroaromatic ring. In addition, as another embodiment, the luminescent body can be considered to be an atomic group (skeleton) containing an aromatic ring having a transition dipole vector on the ring plane.

骨架、啡噻

骨架等。尤其是，具有萘骨架、蒽骨架、茀骨架、

骨架、聯伸三苯骨架、稠四苯骨架、芘骨架、苝骨架、香豆素骨架、喹吖啶酮骨架、萘并雙苯并呋喃骨架的螢光材料是較佳的，因為螢 光量子產率高。 As the condensed aromatic ring or condensed heteroaromatic ring, there can be cited a phenanthrene skeleton, a stilbene skeleton, an acridone skeleton, a phenanthrene ...

Skeleton, Morphothiocyanate

In particular, a naphthalene skeleton, an anthracene skeleton, a fluorene skeleton,

Fluorescent materials with a skeleton, a bis(phenylene) skeleton, a condensed tetraphenyl skeleton, a pyrene skeleton, a perylene skeleton, a coumarin skeleton, a quinacridone skeleton, and a naphthodibenzofuran skeleton are preferred because of their high fluorescence quantum yield.

The protecting group needs to have a triplet excitation energy level higher than the T1 energy level of the luminescent body and the host material. Therefore, it is better to use a saturated hydrocarbon group. This is because the triplet excitation energy level of the substituent without a π bond is high. In addition, the substituent without a π bond does not have the function of transporting carriers (electrons or holes). Therefore, the saturated hydrocarbon group can almost not affect the excited state or carrier transportability of the host material and make the distance between the luminescent body and the host material longer. In addition, in organic compounds containing both substituents without π bonds and substituents with π conjugation, frontier orbitals {HOMO (Highest Occupied Molecular Orbital, also called the highest occupied molecular orbital) and LUMO (Lowest Unoccupied Molecular Orbital, also called the lowest unoccupied molecular orbital)} are often present on the side of the substituent with π conjugation, and in particular, there are many cases where the luminescent body has a frontier orbital. As described later, for energy transfer based on the Dexter mechanism, the overlap of the HOMO of the energy donor and the energy acceptor and the overlap of the LUMO of the energy donor and the energy acceptor are important. Therefore, by using a saturated hydrocarbon group as a protecting group, the distance between the frontier orbital domain of the host material as an energy donor and the frontier orbital domain of the guest material as an energy acceptor can be lengthened, thereby suppressing energy transfer based on the Dexter mechanism.

As a specific example of a protecting group, an alkyl group having 1 to 10 carbon atoms can be cited. Since the distance between the luminescent body and the main material needs to be long, the protecting group is preferably a bulky substituent. Therefore, an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 10 carbon atoms can be applied. In particular, the alkyl group is preferably a bulky branched alkyl group. In addition, the substituent is particularly preferred because it is a bulky substituent when it contains a quaternary carbon.

In addition, it is preferred to have five or more protecting groups relative to one luminophore. By adopting this structure, the entire luminophore can be covered by the protecting groups, so the distance between the host material and the luminophore can be appropriately adjusted. Although FIG. 2B shows a case where the luminophore and the protecting groups are directly bonded, it is more preferred that the protecting groups are not directly bonded to the luminophore. For example, the protecting group may also be bonded to the luminophore via a divalent or higher substituent such as an aryl group or an amine group. By bonding the protecting group to the luminophore via the substituent, the distance between the luminophore and the host material can be effectively lengthened. Therefore, when the luminophore and the protecting group are not directly bonded, by having four or more protecting groups relative to one luminophore, energy transfer based on the Dexter mechanism can be effectively suppressed.

In addition, the divalent or higher substituent that bonds the luminescent body and the protective group is preferably a substituent having π conjugation. By adopting this structure, the physical properties such as the luminescent color, HOMO energy level, and glass transition point of the guest material can be adjusted. In addition, the protective group is preferably arranged so as to be located on the outermost side when the molecular structure is observed with the luminescent body as the center.

〈Examples of fluorescent materials and molecular structures having protective groups〉

Here, the structure of the fluorescent material N,N'-[(2-tert-butylanthracene)-9,10-diyl]-N,N'-bis(3,5-di-tert-butylphenyl)amine (abbreviated as: 2tBu-mmtBuDPhA2Anth) which can be used in a light-emitting element of one embodiment of the present invention, represented by the following structural formula (102) is shown. In 2tBu-mmtBuuDPhA2Anth, the anthracene ring is the luminescent body, and the tert-butyl (tBu) group is used as a protective group.

In FIG3B , the above-mentioned 2tBu-mmtBuDPhA2Anth is represented by a ball-and-stick model. FIG3B shows the situation when 2tBu-mmtBuDPhA2Anth is viewed from the direction of the arrow in FIG3A (the direction horizontal to the anthracene ring plane). The shaded portion in FIG3B represents the portion directly above the anthracene ring plane as the luminescent body, and it can be confirmed that the portion directly above has a region overlapping with the tBu group as the protecting group. For example, in FIG3B , the atom represented by the arrow (a) is the carbon atom of the tBu group overlapping with the shaded portion, and the atom represented by the arrow (b) is the hydrogen atom of the tBu group overlapping with the shaded portion. That is, in 2tBu-mmtBuDPhA2Anth, the atoms constituting the protecting group are located directly on one side of the luminescent body, and the atoms constituting the protecting group are also located directly on the other side of the luminescent body. By adopting this structure, even when the guest material is dispersed in the host material, the distance between the anthracene ring as the luminescent body and the host material can be made long in the plane direction and the vertical direction of the anthracene ring, thereby suppressing the energy transfer based on the Dexter mechanism.

For example, when the migration related to energy transfer is the migration between HOMO and LUMO, for energy transfer based on the Dexter mechanism, the overlap of the HOMO of the host material and the HOMO of the guest material, and the overlap of the LUMO of the host material and the LUMO of the guest material are important. When the HOMO and LUMO of these two materials overlap, the Dexter mechanism occurs significantly. Therefore, in order to suppress the Dexter mechanism, it is important to suppress the overlap of the HOMO and LUMO of the two materials. That is, it is important to make the distance between the skeleton related to the excited state and the host material long. Here, in fluorescent materials, HOMO and LUMO often have a luminescent body. For example, when the HOMO and LUMO of the guest material diffuse above and below the luminescent body surface (above and below the anthracene ring in 2tBu-mmtBuDPhA2Anth), it is important in the molecular structure that the luminescent body surface is covered with a protective group above and below.

In addition, in a fused aromatic ring or fused heteroaromatic ring such as a pyrene ring or anthracene ring used as a luminescent body, a transition dipole vector exists on the ring plane. Therefore, in FIG3B , 2tBu-mmtBuDPhA2Anth preferably has a region overlapping with the tBu group as a protecting group on the surface where the transition dipole vector exists, that is, directly on the surface of the anthracene ring. Specifically, at least one of the atoms constituting the multiple protecting groups (tBu groups in FIG3A and FIG3B ) is located directly on one surface of the fused aromatic ring or the fused heteroaromatic ring (the anthracene ring in FIG3A and FIG3B ), and at least one of the atoms constituting the multiple protecting groups is located directly on another surface of the fused aromatic ring or the fused heteroaromatic ring. By adopting this structure, even when the guest material is dispersed in the host material, the distance between the luminescent body and the host material can be made long, thereby suppressing energy transfer based on the Dexter mechanism. In addition, it is preferable to arrange a protective group such as a tBu group in a manner covering a luminescent body such as anthracene.

〈Structural example 2 of the light-emitting layer〉

FIG4C shows an example of energy level correlation in the light-emitting layer 130 of the light-emitting element 150 of an embodiment of the present invention. The light-emitting layer 130 shown in FIG4A includes compound 131, compound 132, compound 136 and compound 133. In an embodiment of the present invention, compound 132 is preferably a fluorescent material, and compound 136 is preferably a phosphorescent material. In addition, in this structural example, compound 131 and compound 133 are a combination that forms an excited state complex.

As a combination of compound 131 and compound 133, any combination that can form an excited complex is acceptable, and preferably one of the compounds is a compound having a function of transporting holes (hole transportability) and the other is a compound having a function of transporting electrons (electron transportability). In this case, a donor-acceptor type excited complex is easily formed, and the excited complex can be efficiently formed. In addition, when the combination of compound 131 and compound 133 is a combination of a compound having hole transportability and a compound having electron transportability, the balance of carriers can be easily controlled by adjusting their mixing ratio. Specifically, the ratio of compound having hole transportability:compound having electron transportability is preferably in the range of 1:9 to 9:1 (weight ratio). In addition, by having this structure, the balance of carriers can be easily controlled, thereby also making it easy to control the carrier recombination region.

In addition, as a combination of host materials that efficiently forms an excited complex, it is preferred that the HOMO energy level of one of Compound 131 and Compound 133 is higher than the HOMO energy level of the other, and the LUMO energy level of one of them is higher than the LUMO energy level of the other. In addition, the HOMO energy level of Compound 131 may be equal to the HOMO energy level of Compound 133, or the LUMO energy level of Compound 131 may be equal to the LUMO energy level of Compound 133.

Note that the LUMO energy level and the HOMO energy level of a compound can be obtained from the electrochemical properties (reduction potential and oxidation potential) of the compound measured by cyclic voltammetry (CV) measurement.

For example, when compound 131 has hole transportability and compound 133 has electron transportability, as shown in the energy band diagram of FIG4B , it is preferred that the HOMO energy level of compound 131 is higher than the HOMO energy level of compound 133, and the LUMO energy level of compound 131 is higher than the LUMO energy level of compound 133. Due to this energy level correlation, holes and electrons as carriers injected from a pair of electrodes (electrode 101 and electrode 102) are easily injected into compound 131 and compound 133, respectively, which is preferred.

In addition, in Figure 4B, Comp(131) represents compound 131, Comp(133) represents compound 133, _ΔEC1 represents the energy difference between the LUMO energy level and the HOMO energy level of compound 131, _ΔEC3 represents the energy difference between the LUMO energy level and the HOMO energy level of compound 132, and _ΔEE represents the energy difference between the LUMO energy level of compound 133 and the HOMO energy level of compound 131.

In addition, the excited complex formed by Compound 131 and Compound 133 has a molecular orbital of HOMO in Compound 131 and a molecular orbital of LUMO in Compound 133. In addition, the excitation energy of the excited complex is substantially equivalent to the energy difference (ΔE _E ) between the LUMO energy level of Compound 133 and the HOMO energy level of Compound 131, and is smaller than the energy difference (ΔE _C1 ) between the LUMO energy level and the HOMO energy level of Compound 131 and the energy difference (ΔE _C3 ) between the LUMO energy level and the HOMO energy level of Compound 133. Therefore, by forming an excited complex by Compound 131 and Compound 133, an excited state can be formed with a lower excitation energy. In addition, the excited complex can form a stable excited state due to its lower excitation energy.

4C shows the energy level correlation of compound 131, compound 132, and compound 133 in the light-emitting layer 130. The marks and symbols in FIG4C are as follows.

‧Comp(131): Compound 131

‧Comp(133): Compound 133

‧Fluorescent Guest(132): Compound 132

‧S _C1 : S1 energy level of compound 131

_‧TC1 : T1 energy level of compound 131

‧S _C3 : S1 energy level of compound 133

_‧TC3 : T1 energy level of compound 133

_‧SFG : S1 energy level of compound 132

_‧TFG : T1 energy level of compound 132

_‧SE : S1 energy level of the excited complex

_‧TE : T1 energy level of excited complex

In the light-emitting device of one embodiment of the present invention, the compound 131 and the compound 133 included in the light-emitting layer 130 form an excited complex. The S1 energy level ( _SE ) of the excited complex and the T1 energy level ( _TE ) of the excited complex are adjacent energy levels (see path _A9 in FIG4C).

The excitation energy levels ( _SE and _TE ) of the excited complex are lower than the S1 energy levels ( _SC1 and _SC3 ) of the substances forming the excited complex (Compound 131 and Compound 133), so an excited state can be formed with lower excitation energy. Thus, the driving voltage of the light-emitting element 150 can be reduced.

S_FG。在路徑A₁₁中，激態錯合物被用作能量施體，化合物132被用作能量受體。明確而言，較佳的是，在激態錯合物的螢光光譜的短波長一側的尾處劃切線，將該外推線的波長的能量設定為S_E，將化合物132的吸收光譜的吸收端的波長的能量設定為S_FG，此時滿足S_E

S_FG。此外，由於化合物136是磷光材料，所以能夠接收激態錯合物所具有的單重激發能及三重激發能(圖4C的路徑A₁₂)。也就是說，有可能發生從S_E及T_E到T_PG的能量轉移。此時，較佳為滿足S_E

T_PG及T_E

T_PG。此外，當S_FG

T_PG時，化合物132所具有的單重激發能被轉換為螢光發光的過程與被轉移到T_PG的過程(圖4C的路徑A₅)競爭。化合物136能夠藉由路徑A₁₂及A₅接收激發能。因此，可以從發光層130得到化合物132和化合物136兩者的發光。 Since the S1 energy level ( _SE ) and T1 energy level ( _TE ) of the excited complex are adjacent energy levels, antisystem crossing is easily generated and the excited complex has TADF characteristics. Therefore, the excited complex has the function of converting triplet excitation energy into singlet excitation energy by upconversion (path _A10 in FIG. 4C). The singlet excitation energy of the excited complex can be quickly transferred to compound 132 (path _A11 in FIG. 4C). At this time, it is better to satisfy SE _.

In _{path A11} , the excited complex is used as an energy donor and compound 132 is used as an energy acceptor. Specifically, it is preferred that a tangent line is drawn at the tail of the short-wavelength side of the fluorescence spectrum of the excited complex, the energy of the wavelength of the extrapolated line is set as _SE , and the energy of the wavelength at the absorption end of the absorption spectrum of compound 132 is set as S _FG , and SE is satisfied _.

S _FG . In addition, since compound 136 is a phosphorescent material, it can receive the singlet excitation energy and triplet excitation energy of the excited complex (path A ₁₂ in FIG. 4C ). In other words, energy transfer from S _E and T _E to T _PG may occur. In this case, it is preferred to satisfy S _E

_TPG and _TE

T _PG . In addition, when S _FG

When _TPG , the process of converting the singlet excitation energy of compound 132 into fluorescent luminescence competes with the process of transferring to _TPG (path _A5 in FIG4C ). Compound 136 can receive excitation energy through paths _A12 and _A5 . Therefore, luminescence of both compound 132 and compound 136 can be obtained from the luminescent layer 130.

Although not shown, energy transfer from Compound 131 and Compound 133 to Compound 132 and/or Compound 136 may also occur.

0.2eV且S_E-T_C3

0.2eV。 In order to improve the TADF characteristics, it is preferred that the T1 energy level of compound 131 and compound 133, that is, T _C1 and T _C3, is greater than _TE . As an indicator, it is preferred that the emission peak wavelength on the shortest wavelength side of the phosphorescence spectrum of compound 131 and compound 133 is less than the maximum emission peak wavelength of the excited complex. Alternatively, it is preferred that a tangent line is drawn at the tail of the short wavelength side of the fluorescence spectrum of the excited complex, and the energy of the wavelength of the extrapolated line is set to _SE , and a tangent line is drawn at the tail of the short wavelength side of the phosphorescence spectrum of compound 131 and compound 133, respectively, and the energy of the wavelength of the extrapolated line is set to T _C1 and T _C3 of each compound, and _SE -T _C1 is preferred in this case.

0.2eV and S _E -T _C3

0.2eV.

The triplet excitation energy generated in the light-emitting layer 130 passes through the above-mentioned path _A9 and energy transfer from the S1 energy level of the excited complex to the S1 energy level of the compound 132 (path _A11 ), thereby making the compound 132 emit light. Therefore, by using a combination of materials that form an excited complex for the light-emitting layer 130, the light-emitting efficiency of the light-emitting element can be improved.

Here, in a light-emitting element of one embodiment of the present invention, a fluorescent material whose light-emitting body has a protective group is used for compound 132. By adopting this structure, as described above, energy transfer based on the Dexter mechanism represented by paths _A13 and _A6 can be suppressed, and deactivation of triplet excitation energy can be suppressed. Therefore, a light-emitting element with high light-emitting efficiency can be obtained.

In this specification, the process of the above-mentioned path _A9 to _A11 is sometimes referred to as ExSET (Exciplex-Singlet Energy Transfer) or ExEF (Exciplex-Enhanced Fluorescence). In other words, in the light-emitting layer 130, the excitation energy is supplied from the exciplex to the fluorescent material.

〈Structural example 3 of the light-emitting layer〉

In this structural example, a case where a phosphorescent material is used as compound 133 of the light-emitting element using the ExEF described above is described. That is, a case where a phosphorescent material is used as one of the compounds that form an exciplex is described.

S_FG。 In this structural example, a compound containing a heavy atom is used as one of the compounds forming the excited state complex. Therefore, the intersystem crossing between the singlet excited state and the triplet excited state is promoted. Therefore, an excited state complex capable of transitioning from the triplet excited state to the singlet ground state (that is, capable of exhibiting phosphorescence) can be formed. At this time, unlike a general excited state complex, the triplet excitation energy level ( _TE ) of the excited state complex is the energy level of an energy donor, so _TE is preferably higher than the singlet excitation energy level ( _SFG ) of compound 132 as a luminescent material. Specifically, it is preferred that a tangent line be drawn at the tail of the emission spectrum of the excited complex using heavy atoms on the short wavelength side, the energy of the wavelength of the extrapolated line be set as _TE , and the energy of the wavelength of the absorption end of the absorption spectrum of compound 132 be set as _SFG , and then TE is satisfied _.

S _{F G} .

In the case of such energy level correlation, the triplet excitation energy of the generated excited complex can be transferred from the triplet excitation energy level ( _TE ) of the excited complex to the singlet excitation energy level ( _SFG ) of compound 132. Note that the S1 energy level ( _SE ) and the T1 energy level ( _TE ) of the excited complex are adjacent to each other, so that it is sometimes difficult to clearly distinguish between fluorescence and phosphorescence in the emission spectrum. In this case, fluorescence and phosphorescence can sometimes be distinguished based on the luminescence lifetime.

The phosphorescent material used in the above structure preferably contains heavy atoms such as Ir, Pt, Os, Ru, Pd, etc. On the other hand, in the present structural example, the compound 133 of the phosphorescent material is also used as an energy donor, so its quantum yield can be either high or low. That is, the energy transfer from the triplet excitation energy level of the excited complex to the singlet excitation energy level of the fluorescent material is an allowed transition. In the energy transfer from the excited complex composed of the above phosphorescent material or the above phosphorescent material to the fluorescent material, the energy transfer from the triplet excitation energy level of the energy donor to the singlet excitation energy level of the guest material (energy acceptor) is an allowed transition, so it is preferred. Therefore, the triplet excitation energy of the excited complex can be transferred to the S1 energy level ( _SFG ) of the guest material through the process of path _A11 without going through the process of path _A10 in FIG. _4C . That is, the triplet excitation energy and the singlet excitation energy can be transferred to the S1 energy level of the guest material only through the processes of path A9 and path _A11 . In path _A11 , the excited complex is used as an energy donor, and compound 132 and/or compound 136 is used as an energy acceptor.

Here, in a light-emitting element of one embodiment of the present invention, a fluorescent material whose light-emitting body has a protective group is used for compound 132. By adopting this structure, as described above, energy transfer based on the Dexter mechanism represented by paths _A13 and _A6 can be suppressed, and deactivation of triplet excitation energy can be suppressed. Therefore, a light-emitting element with high light-emitting efficiency can be obtained.

〈Structural Example 4 of the Light Emitting Layer〉

In this structural example, FIG. 4D is used to illustrate the case where a material having TADF characteristics is used as the compound 133 of the light-emitting element using the ExEF described above.

S_FG。 Since compound 133 is a TADF material, compound 133 without forming an excited complex has the function of converting triplet excitation energy into singlet excitation energy by upconversion (path A ₁₄ in FIG. 4D ). The singlet excitation energy of compound 133 can be quickly transferred to compound 132 (path A ₁₅ in FIG. 4D ). At this time, it is preferred that _SC3

S _{F G} .

Similar to the structural example of the light-emitting layer, in the light-emitting element of one embodiment of the present invention, there are paths for triplet excitation energy to be transferred to compound 132 as a fluorescent material via paths _A9 to _A11 in FIG4D , and there are paths for triplet excitation energy to be transferred to compound 132 via paths _A14 and _A15 in FIG4D . Since there are multiple paths for triplet excitation energy to be transferred to the fluorescent material, the light-emitting efficiency can be further improved.

Although not shown, energy transfer may also occur from Compound 131 to Compound 132 and/or Compound 136. Energy transfer may also occur from Compound 133 to Compound 136.

〈Structural Example 5 of the Light Emitting Layer〉

FIG5B shows an example of energy level correlation in the light-emitting layer 130 of the light-emitting element 150 of an embodiment of the present invention. The light-emitting layer 130 in FIG5A includes compound 131, compound 132, compound 136 and compound 133. In an embodiment of the present invention, compound 132 is a fluorescent material having a protective group, and compound 136 is a phosphorescent material. Compound 133 has the function of converting triplet excitation energy into luminescence. In this structural example, the description is based on the premise that compound 133 is a phosphorescent material. The marks and symbols in FIG5B are the same as those shown in FIG4C.

T_C1的關係的材料，可以將在化合物131中產生的單重激發能及三重激發能都轉移到化合物133的T_C3能階(圖5B中的路徑A₁₆)。注意，一部分載子有可能在化合物133中再結合。 In the light-emitting device of one embodiment of the present invention, since the recombination of carriers mainly occurs in the compound 131 included in the light-emitting layer 130, singlet excitons and triplet excitons are generated. Since the compound 133 here is a phosphorescent material, by selecting a material that satisfies _TC3

The materials with a T _C1 relationship can transfer both the singlet excitation energy and triplet excitation energy generated in compound 131 to the T _C3 energy level of compound 133 (path A ₁₆ in FIG. 5B ). Note that some carriers may be recombined in compound 133.

S_FG的情況下，化合物133的激發能高效地轉移到作為客體材料的化合物132的單重激發態，所以是較佳的。明確而言，較佳的是，在化合物133的磷光光譜的短波長一側的尾處劃切線，將該外推線的波長的能量設定為T_C3，將化合物132的吸收光譜的吸收端的波長的能量設定為S_FG，此時滿足T_C3

S_FG。此外，由於化合物136是磷光材料，所以能夠接收化合物133所具有的三重激發能(圖5B的路徑A₁₈)。也就是說，有可能發生從T_C3到T_PG的能量轉移。此時，較佳為T_C3

T_PG。此外，當S_FG

T_PG時，化合物132所具有的單重激發能被轉換為螢光發光的過程與被轉移到T_PG的過程(圖5B的路徑A₅)競爭。化合物136能夠藉由路徑A₁₈及A₅接收激發能。因此，可以從發光層130得到化合物132和化合物136兩者的發光。 The phosphorescent material used in the above structure preferably contains heavy atoms such as Ir, Pt, Os, Ru, Pd, etc. On the other hand, as described above, in the present structural example, the compound 133 of the phosphorescent material is also used as an energy donor, so its quantum yield can be either high or low. When the phosphorescent material is used as the compound 133 phosphorescent material, the energy transfer from the triplet excitation energy level of the energy donor to the singlet excitation energy level of the guest material (energy acceptor) is an allowed transition, so it is preferred. Therefore, the triplet excitation energy of compound 133 can be transferred to the S1 energy level ( _SFG ) of the guest material through the process of path A _17. In path A ₁₇ , compound 133 is used as an energy donor and compound 132 is used as an energy acceptor. At this time, while satisfying _TC3

In the case of _SFG , the excitation energy of compound 133 is efficiently transferred to the singlet excited state of compound 132 as the guest material, so it is preferred. Specifically, it is preferred to draw a tangent line at the tail of the short-wavelength side of the phosphorescence spectrum of compound 133, set the energy of the wavelength of the extrapolated line to _TC3 , and set the energy of the wavelength of the absorption end of the absorption spectrum of compound 132 to _SFG , and then satisfy _TC3

_In addition, since compound 136 is a phosphorescent material, it can receive the triplet excitation energy of compound 133 (path A ₁₈ in FIG. 5B ). In other words, energy transfer from T _C3 to T _PG may occur. In this case, T _C3 is preferably

T _PG . In addition, when S _FG

When _TPG , the process of converting the singlet excitation energy of compound 132 into fluorescent luminescence competes with the process of transferring to _TPG (path _A5 in FIG5B ). Compound 136 can receive excitation energy through paths _A18 and _A5 . Therefore, luminescence of both compound 132 and compound 136 can be obtained from the luminescent layer 130.

In addition, although not shown, energy transfer from compound 131 to compound 132 and/or compound 136 may also occur.

Here, in a light-emitting element of one embodiment of the present invention, a guest material whose light-emitting body has a protecting group is used for compound 132. By adopting this structure, as described above, energy transfer based on the Dexter mechanism represented by the paths _A19 and _A6 can be suppressed, and deactivation of triplet excitation energy can be suppressed. Therefore, a fluorescent light-emitting element with high light-emitting efficiency can be obtained.

〈Structural Example 6 of the Light Emitting Layer〉

FIG5C shows an example of the energy level correlation in the light-emitting layer 130 of the light-emitting element 150 of an embodiment of the present invention. The light-emitting layer 130 in FIG5C includes compound 131, compound 132, compound 136 and compound 133. In an embodiment of the present invention, compound 132 is a fluorescent material having a protective group, and compound 136 is a phosphorescent material. Compound 133 has the function of converting triplet excitation energy into luminescence. In this structural example, the explanation is based on the premise that compound 133 is a compound having TADF characteristics. The marks and symbols in FIG5C are the same as those shown in FIG4C.

S_C1及T_C3

T_C1的關係的材料，可以將在化合物131中產生的單重激發能及三重激發能都轉移到化合物133的S_C3能階及T_C3能階(圖5C中的路徑A₂₀)。注意，一部分載子有可能在化合物133中再結合。 In the light-emitting device of one embodiment of the present invention, since carrier recombination mainly occurs in the compound 131 included in the light-emitting layer 130, singlet excitons and triplet _excitons are generated.

S _C1 and T _C3

The materials with a T _C1 relationship can transfer the singlet excitation energy and triplet excitation energy generated in compound 131 to the S _C3 energy level and T _C3 energy level of compound 133 (path A ₂₀ in FIG. 5C ). Note that some carriers may be recombined in compound 133.

S_FG。明確而言，較佳的是，在化合物133的螢光光譜的短波長一側的尾處劃切線，將該外推線的波長的能量設定為S_C3，將化合物132的吸收光譜的吸收端的波長的能量設定為S_FG，此時滿足S_C3

S_FG。經過路徑A₂₀至路徑A₂₂的過程，由此可以將發光層130中的三重激發能轉換為化合物132的螢光發光。在路徑A₂₂中，化合物133被用作能量施體，化合物132被用作能量受體。此外，由於化合物136是磷光材料，所以能夠接收化合物133所具有的單重激發能及三重激發能(圖5C的路徑A₂₃)。也就是說，有可能發生從S_C3及T_C3到T_PG的能量轉移。此外，當S_FG

T_PG時，化合物132所具有的單重激發能被轉換為螢光發光的過程與被轉移到T_PG的過程(圖5C的路徑A₅)競爭。化合物136能夠藉由路徑A₂₃及A₅接收激發能。因此，可以從發光層130得到化合物132和化合物136兩者的發光。 Here, since compound 133 is a TADF material, compound 133 has the function of converting triplet excitation energy into singlet excitation energy by up-conversion (path A ₂₁ in FIG. 5C ). The singlet excitation energy of compound 133 can be quickly transferred to compound 132 (path A ₂₂ in FIG. 5C ). At this time, it is preferred to satisfy _SC3

Specifically, it is preferred that a tangent line is drawn at the tail of the short-wavelength side of the fluorescence spectrum of compound 133, the energy of the _wavelength of the extrapolated line is set to _SC3 , and the energy of the wavelength at the absorption end of the absorption spectrum of compound 132 is set to _SC3 . At this time, _SC3 is satisfied.

S _FG . Through the process from path A ₂₀ to path A ₂₂ , the triplet excitation energy in the light-emitting layer 130 can be converted into the fluorescent luminescence of compound 132. In path A ₂₂ , compound 133 is used as an energy donor and compound 132 is used as an energy acceptor. In addition, since compound 136 is a phosphorescent material, it can receive the singlet excitation energy and triplet excitation energy possessed by compound 133 (path A ₂₃ in FIG. 5C ). In other words, energy transfer from S _C3 and T _C3 to T _PG may occur. In addition, when S _FG

When _TPG , the process of converting the singlet excitation energy of compound 132 into fluorescent luminescence competes with the process of transferring to _TPG (path _A5 in FIG5C ). Compound 136 can receive excitation energy through paths _A23 and _A5 . Therefore, luminescence of both compound 132 and compound 136 can be obtained from the luminescent layer 130.

In addition, although not shown, energy transfer from compound 131 to compound 132 and/or compound 136 may also occur.

Here, in a light-emitting element of one embodiment of the present invention, a guest material whose light-emitting body has a protecting group is used for compound 132. By adopting this structure, as described above, energy transfer based on the Dexter mechanism represented by paths A ₂₄ and A ₆ can be suppressed, and deactivation of triplet excitation energy can be suppressed. Therefore, a fluorescent light-emitting element with high light-emitting efficiency can be obtained.

Energy transfer mechanism

The Foster mechanism and the Dexter mechanism are described below. Although the energy transfer process between the molecules of the first material and the second material is described here in relation to the supply of excitation energy from the first material in an excited state to the second material in a ground state, the same is true when either of the above is an excited complex.

Foster Mechanism

In the Förster mechanism, direct contact between molecules is not required for energy transfer, and energy transfer occurs through the resonance phenomenon of dipole oscillation between the first material and the second material. Through the resonance phenomenon of dipole oscillation, the first material supplies energy to the second material, the excited state of the first material becomes the ground state, and the ground state of the second material becomes the excited state. In addition, the rate constant k _h*→g of the Förster mechanism is shown in formula (1).

In formula (1), ν represents the oscillation number, _f'h (ν) represents the normalized emission spectrum of the first material (fluorescence spectrum when discussing energy transfer from a singlet excited state, and phosphorescence spectrum when discussing energy transfer from a triplet excited state), _εg (ν) represents the molar absorption coefficient of the second material, N represents the Avogadro number, n represents the refractive index of the medium, R represents the molecular distance between the first material and the second material, τ represents the measured lifetime of the excited state (fluorescence lifetime or phosphorescence lifetime), c represents the speed of light, Φ represents the luminescence quantum yield (fluorescence quantum yield when discussing energy transfer from a singlet excited state, and phosphorescence quantum yield when discussing energy transfer from a triplet excited state), and ^K2 represents the coefficient of the orientation of the transition dipole moments of the first material and the second material (0 to 4). In addition, in the random alignment, K ² =2/3.

Dexter Mechanism

In the Dexter mechanism, the first material and the second material are close to the contact effective distance that produces the overlap of the orbital domains, and energy transfer occurs by exchanging the electrons of the excited state of the first material and the electrons of the ground state of the second material. In addition, the rate constant k _h*→g of the Dexter mechanism is shown in formula (2).

In formula (2), h represents Planck's constant, K represents a constant having an energy dimension, ν represents the oscillation number, f' _h (ν) represents the normalized emission spectrum of the first material (fluorescence spectrum when discussing energy transfer from a singlet excited state, phosphorescence spectrum when discussing energy transfer from a triplet excited state), ε' _g (ν) represents the normalized absorption spectrum of the second material, L represents the effective molecular radius, and R represents the molecular distance between the first material and the second material.

Here, the energy transfer efficiency Φ _ET from the first material to the second material is expressed by formula (3). _{k r} represents the rate constant of the luminescence process of the first material (fluorescence when discussing energy transfer from a singlet excited state, phosphorescence when discussing energy transfer from a triplet excited state), k _n represents the rate constant of the non-luminescence process (thermal deactivation or intersystem hopping) of the second material, and τ represents the lifetime of the excited state of the first material measured.

From formula (3), we can see that in order to improve the energy transfer efficiency Φ _ET , the energy transfer rate constant k _h*→g can be increased to make other competing rate constants k _r +k _n (=1/τ) relatively smaller.

〈〈Concepts used to enhance energy transfer〉〉

First, consider the energy transfer based on the Förster mechanism. By substituting formula (1) into formula (3), τ can be eliminated. Therefore, in the Förster mechanism, the energy transfer efficiency Φ _ET does not depend on the lifetime τ of the excited state of the first material. In addition, when the luminescence quantum yield Φ is high, it can be said that the energy transfer efficiency Φ _ET is high.

In addition, the overlap between the emission spectrum of the first material and the absorption spectrum of the second material (equivalent to the absorption of the transition from the singlet ground state to the singlet excited state) is preferably large. Furthermore, the molar absorption coefficient of the second material is preferably high. This means that the emission spectrum of the first material overlaps with the absorption band that appears on the longest wavelength side of the second material. Note that since the direct transition from the singlet ground state to the triplet excited state is prohibited in the second material, the molar absorption coefficient in the triplet excited state is so small that it can be ignored in the second material. Therefore, the energy transfer process from the excited state of the first material to the triplet excited state of the second material based on the Förster mechanism can be ignored, and only the energy transfer process to the singlet excited state of the second material needs to be considered.

In addition, according to formula (1), the energy transfer rate based on the Foster mechanism is inversely proportional to the sixth power of the molecular distance R between the first material and the second material. As described above, when R is less than 1 nm, the energy transfer based on the Dexter mechanism is dominant. Therefore, in order to suppress the energy transfer based on the Dexter mechanism while increasing the energy transfer rate based on the Foster mechanism, the molecular distance is preferably greater than 1 nm and less than 10 nm. Therefore, the above-mentioned protecting group is required not to be too large, and the number of carbon atoms constituting the protecting group is preferably greater than 3 and less than 10.

Next, consider the energy transfer based on the Dexter mechanism. From formula (2), it can be seen that in order to increase the rate constant k _h*→g , the overlap between the emission spectrum of the first material (the fluorescence spectrum when discussing the energy transfer from the singlet excited state, and the phosphorescence spectrum when discussing the energy transfer from the triplet excited state) and the absorption spectrum of the second material (equivalent to the absorption of the transition from the singlet ground state to the singlet excited state) is preferably large. Therefore, the energy transfer efficiency can be optimized by overlapping the emission spectrum of the first material with the absorption band on the longest wavelength side of the second material.

In addition, when formula (2) is substituted into formula (3), it can be seen that the energy transfer efficiency Φ _ET in the Dexter mechanism depends on τ. Since the Dexter mechanism is an energy transfer process based on electron exchange, energy transfer from the triplet excited state of the first material to the triplet excited state of the second material also occurs in the same manner as energy transfer from the singlet excited state of the first material to the singlet excited state of the second material.

In the light-emitting element of an embodiment of the present invention, the second material is a fluorescent material, so the energy transfer efficiency of the triplet excited state to the second material is preferably low. In other words, the energy transfer efficiency based on the Dexter mechanism from the first material to the second material is preferably low, and the energy transfer efficiency based on the Foster mechanism from the first material to the second material is preferably high.

As described above, the energy transfer efficiency based on the Foster mechanism does not depend on the lifetime τ of the excited state of the first material. On the other hand, the energy transfer efficiency based on the Dexter mechanism depends on the excitation lifetime τ of the first material. In order to reduce the energy transfer efficiency based on the Dexter mechanism, the excitation lifetime τ of the first material is preferably short.

Therefore, in one embodiment of the present invention, an excited state complex, a phosphorescent material or a TADF material is used as the first material. These materials have the function of converting triplet excitation energy into luminescence. The energy transfer efficiency of the Förster mechanism depends on the luminescence quantum yield of the energy donor. Therefore, the first material such as a phosphorescent material, an excited state complex or a TADF material that can convert the energy of the triplet excited state into luminescence can utilize the Förster mechanism to transfer its excitation energy to the second material. On the other hand, by means of the structure of one embodiment of the present invention, the antisystem transition from the triplet excited state to the singlet excited state of the first material (excited state complex or TADF material) can be promoted, and the excitation lifetime τ of the triplet excited state of the first material can be shortened. In addition, the transition from the triplet excited state to the singlet ground state of the first material (phosphorescent material or excited complex using the phosphorescent material) can be promoted, and the excitation lifetime τ of the triplet excited state of the first material can be shortened. As a result, the energy transfer efficiency based on the Dexter mechanism from the triplet excited state of the first material to the triplet excited state of the fluorescent material (second material) can be reduced.

In a light-emitting element of an embodiment of the present invention, as described above, a fluorescent material having a protective group is used as the second material. Therefore, the molecular distance between the first material and the second material can be made large. Therefore, in a light-emitting element of an embodiment of the present invention, by using a material having a function of converting triplet excitation energy into luminescence as the first material and using a fluorescent material having a protective group as the second material, the energy transfer efficiency based on the Dexter mechanism can be reduced. As a result, the radiationless deactivation of the triplet excitation energy in the light-emitting layer 130 can be suppressed, thereby providing a light-emitting element with high luminescence efficiency.

<Material>

Next, the components of a light-emitting element according to an embodiment of the present invention are described.

〈〈Luminous layer〉〉

The following describes the materials that can be used for the light-emitting layer 130. In the light-emitting layer of the light-emitting element of one embodiment of the present invention, an energy acceptor having the function of converting triplet excitation energy into light emission and an energy donor having a protective group in the light-emitting body are used. As the material having the function of converting triplet excitation energy into light emission, TADF characteristic materials and phosphorescent materials can be cited.

骨架、啡噻

骨架等。尤其是，具有萘骨架、蒽骨架、茀骨架、

骨架、聯伸三苯骨架、稠四苯骨架、芘骨架、苝骨架、香豆素骨架、喹吖啶酮骨架、萘并雙苯并呋喃骨架的螢光化合物具有高螢光量子產率，所以是較佳的。 Examples of the luminescent material of compound 132 used as an energy acceptor include a phenanthrene skeleton, a stilbene skeleton, an acridone skeleton, a phenanthrene skeleton, a stilbene skeleton, a phenanthrene ...

Skeleton, Morphothiocyanate

In particular, a naphthalene skeleton, an anthracene skeleton, a fluorene skeleton,

Fluorescent compounds with a skeleton, a triphenyl skeleton, a condensed tetraphenyl skeleton, a pyrene skeleton, a perylene skeleton, a coumarin skeleton, a quinacridone skeleton, and a naphthodibenzofuran skeleton have high fluorescence quantum yields and are therefore preferred.

In addition, the protecting group is preferably an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 3 to 10 carbon atoms, a branched alkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms.

Examples of the alkyl group having 1 to 10 carbon atoms include methyl, ethyl, propyl, pentyl, and hexyl groups, and particularly preferred are branched alkyl groups having 3 to 10 carbon atoms described below. Note that the alkyl group is not limited thereto.

As the cycloalkyl group having 3 or more and 10 or less carbon atoms, cyclopropyl, cyclobutyl, cyclohexyl, norbornyl, adamantyl, etc. can be mentioned. The cycloalkyl group is not limited thereto. In addition, when the cycloalkyl group has a substituent, as the substituent, alkyl groups having 1 to 7 carbon atoms such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, dibutyl, tertiary butyl, pentyl and hexyl, cycloalkyl groups having 5 to 7 carbon atoms such as cyclopentyl, cyclohexyl, cycloheptyl and 8,9,10-trinorbornyl, and aryl groups having 6 to 12 carbon atoms such as phenyl, naphthyl and biphenyl can be mentioned.

Examples of the branched alkyl group having 3 to 10 carbon atoms include isopropyl, dibutyl, isobutyl, tertiary butyl, isopentyl, dipentyl, tertiary pentyl, neopentyl, isohexyl, 3-methylpentyl, 2-methylpentyl, 2-ethylbutyl, 1,2-dimethylbutyl, and 2,3-dimethylbutyl. The branched alkyl group is not limited thereto.

Examples of the trialkylsilyl group having 3 to 12 carbon atoms include trimethylsilyl, triethylsilyl, tertiary butyldimethylsilyl, etc. The trialkylsilyl group is not limited thereto.

In addition, as the molecular structure of the energy acceptor, it is preferred that the luminescent body is bonded to two or more diarylamine groups and each aryl group possessed by the diarylamine group has at least one protecting group. It is more preferred that at least two protecting groups are bonded to each aryl group. This is because: the more the number of protecting groups, the greater the effect of suppressing the energy transfer based on the Dexter mechanism when the guest material is used in the luminescent layer. In order to suppress the increase of molecular weight and maintain sublimation, the diarylamine group is preferably a diphenylamine group.

By bonding two or more diarylamine groups to the luminescent body, a fluorescent material with high quantum yield can be obtained while adjusting the luminescent color. In addition, the diarylamine groups are preferably bonded to positions symmetrical with respect to the luminescent body. By adopting this structure, a fluorescent material with high quantum yield can be realized.

In addition, the protecting group may be bonded to the luminescent body via the aryl group of the diarylamine group, rather than being directly bonded to the luminescent body. By adopting this structure, the protecting group can be arranged in a manner covering the luminescent body, so the distance between the main material and the luminescent body can be made long from all directions, which is preferred. In addition, when the protecting group is not directly bonded to the luminescent body, it is preferred to bond four or more protecting groups to one luminescent body.

In addition, as shown in FIG3A and FIG3B, it is preferred that at least one of the atoms constituting the plurality of protecting groups is located directly on the luminescent body, that is, directly on one face of the fused aromatic ring or the fused heteroaromatic ring, and at least one of the atoms constituting the plurality of protecting groups is located directly on another face of the fused aromatic ring or the fused heteroaromatic ring. As a specific method, the following structure can be cited. That is, the fused aromatic ring or the fused heteroaromatic ring of the luminescent body is bonded to two or more diphenylamine groups, and the phenyl groups in the two or more diphenylamine groups have protecting groups at the 3-position and the 5-position, respectively, independently.

By adopting such a structure, as shown in FIG3A and FIG3B , a configuration can be achieved in which the protecting group at the 3-position or 5-position on the phenyl group is located directly above the condensed aromatic ring or condensed heteroaromatic ring that is the luminescent body. As a result, the upper and lower surfaces of the condensed aromatic ring or the condensed heteroaromatic ring can be efficiently covered, and energy transfer based on the Dexter mechanism can be suppressed.

As the energy acceptor material as described above, for example, an organic compound represented by the following general formula (G1) or (G2) can be used.

[Chemical formula 2]

In the general formulae (G1) and (G2), A represents a substituted or unsubstituted fused aromatic ring having 10 to 30 carbon atoms or a substituted or unsubstituted fused heteroaromatic ring having 10 to 30 carbon atoms, ^Ar1 to ^Ar6 each independently represent a substituted or unsubstituted aromatic hydrocarbon group having 6 to 13 carbon atoms, ^X1 to ^X12 each independently represent any one of a branched alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 10 carbon atoms. ^R1 to ^R10 each independently represent any one of hydrogen, an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms.

As the aromatic hydrocarbon group having 6 to 13 carbon atoms, phenyl, biphenyl, naphthyl, fluorenyl, etc. can be cited. Note that the aromatic hydrocarbon group is not limited thereto. In addition, when the aromatic hydrocarbon group has a substituent, as the substituent, alkyl groups having 1 to 7 carbon atoms such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, dibutyl, tertiary butyl, pentyl, hexyl, etc., cycloalkyl groups having 5 to 7 carbon atoms such as cyclopentyl, cyclohexyl, cycloheptyl, 8,9,10-trinorbornyl, phenyl, naphthyl, biphenyl, etc., aryl groups having 6 to 12 carbon atoms, etc. can be cited.

In the general formula (G1), a substituted or unsubstituted fused aromatic ring having 10 to 30 carbon atoms or a substituted or unsubstituted fused heteroaromatic ring having 10 to 30 carbon atoms represents the above-mentioned luminescent body, and the above-mentioned skeleton can be used. In the general formulas (G1) and (G2), ^X1 to ^X12 represent a protecting group.

In general formula (G2), the protecting group is bonded to the quinacridone skeleton, which is the luminescent body, via the aromatic group. By adopting this structure, the protecting group can be arranged in a manner covering the luminescent body, so that energy transfer based on the Dexter mechanism can be suppressed. In addition, the protecting group can also be directly bonded to the luminescent body.

As the energy acceptor material, an organic compound represented by the following general formula (G3) or (G4) can be used.

In the general formulae (G3) and (G4), A represents a substituted or unsubstituted fused aromatic ring having 10 to 30 carbon atoms or a substituted or unsubstituted fused heteroaromatic ring having 10 to 30 carbon atoms, and ^X1 to ^X12 each independently represent any one of a branched alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 10 carbon atoms.

The protecting group is preferably bonded to the luminescent body through the phenyl group. By adopting this structure, the protecting group can be arranged in a manner to cover the luminescent body, so that energy transfer based on the Dexter mechanism can be suppressed. In addition, when the luminescent body and the protecting group are bonded through the phenyl group and two protecting groups are bonded to the phenyl group, as shown in general formulas (G3) and (G4), the two protecting groups are preferably bonded to the phenyl group in the meta position. By adopting this structure, the luminescent body can be efficiently covered, so energy transfer based on the Dexter mechanism can be suppressed. As an example of an organic compound represented by general formula (G3), the above-mentioned 2tBu-mmtBuDPhA2Anth can be cited. That is, in one embodiment of the present invention, general formula (G3) is a particularly preferred example.

As the energy acceptor material, an organic compound represented by the following general formula (G5) can be used.

[Chemical formula 4]

In the general formula (G5), ^X1 to ^X8 each independently represent any one of a branched alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 10 carbon atoms, and ^R11 to ^R18 each independently represent any one of hydrogen, a branched alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, a trialkylsilyl group having 3 to 10 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 25 carbon atoms.

Examples of the aryl group having 6 to 25 carbon atoms include phenyl, naphthyl, biphenyl, fluorenyl, and spirofluorenyl. Note that the aryl group having 6 to 25 carbon atoms is not limited thereto. When the aryl group has a substituent, examples of the substituent include an alkyl group having 1 to 10 carbon atoms, a branched alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 10 carbon atoms.

Anthracene compounds have high light emission quantum yields and their light emitting bodies have small areas, so the upper and lower surfaces of anthracene can be efficiently covered with protective groups. An example of an organic compound represented by general formula (G5) is the above-mentioned 2tBu-mmtBuDPhA2Anth.

Examples of the compounds listed in the general formulae (G1) to (G5) are shown below by structural formulae (102) to (105) and (200) to (284). Note that the compounds listed in the general formulae (G1) to (G5) are not limited thereto. In addition, the compounds represented by structural formulae (102) to (105) and (200) to (284) can be appropriately used as a guest material of a light-emitting element of an embodiment of the present invention. Note that the guest material is not limited thereto.

[Chemical formula 6]

[Chemical formula 7]

[Chemical formula 8]

[Chemical formula 9]

[Chemical formula 10]

[Chemical formula 11]

[Chemical formula 12]

[Chemical formula 13]

[Chemical formula 14]

[Chemical formula 15]

[Chemical formula 16]

[Chemical formula 17]

[Chemical formula 18]

[Chemical formula 19]

[Chemical formula 20]

[Chemical formula 21]

[Chemical formula 22]

[Chemical formula 23]

[Chemical formula 24]

[Chemical formula 25]

[Chemical formula 26]

Structural formulas (100) and (101) show examples of materials that can be suitably used as a guest material of a light-emitting device according to an embodiment of the present invention. Note that the guest material is not limited thereto.

[Chemical formula 27]

When compound 133 is used as an energy donor, for example, a TADF material can be used. Preferably, the energy difference between the S1 energy level and the T1 energy level of compound 133 is small, specifically, greater than 0 eV and less than 0.2 eV. In addition, a TADF material can also be used as compound 136.

Compound 133 and/or Compound 136 preferably include a skeleton having hole transport properties and a skeleton having electron transport properties. Alternatively, Compound 133 and/or Compound 136 preferably include a π-electron-rich skeleton or an aromatic amine skeleton and a π-electron-deficient skeleton. This makes it easy to form a donor-acceptor type excited state in the molecule. Furthermore, it is preferred that a structure in which a skeleton having electron transport properties is directly bonded to a skeleton having hole transport properties in a manner that simultaneously enhances the donor and acceptor properties in the molecule of Compound 133 and/or Compound 136. Alternatively, it is preferred that a structure in which a π-electron-rich skeleton or an aromatic amine skeleton is directly bonded to a π-electron-deficient skeleton. By enhancing both the donor property and the acceptor property in the molecule, the overlapped region of the HOMO molecular orbital distribution and the LUMO molecular orbital distribution can be reduced in Compound 133 and/or Compound 136, thereby reducing the energy difference between the singlet excitation energy level and the triplet excitation energy level of Compound 133 and/or Compound 136. In addition, the triplet excitation energy level of Compound 133 and/or Compound 136 can be maintained high.

When the TADF material is composed of one material, for example, the following materials can be used.

First, fullerene or its derivatives, acridine derivatives such as proflavine, eosin, etc. Also, metal-containing porphyrins containing magnesium (Mg), zinc (Zn), cadmium (Cd), tin (Sn), platinum (Pt), indium (In), or palladium (Pd) can be cited. Examples of the metal-containing porphyrin include protoporphyrin-tin fluoride complex (SnF ₂ (Proto IX)), mesoporphyrin-tin fluoride complex (SnF ₂ (Meso IX)), hematoporphyrin-tin fluoride complex (SnF ₂ (Hemato IX)), tetramethylnaphthoporphyrin-tin fluoride complex (SnF ₂ (Copro III-4Me)), octaethylporphyrin-tin fluoride complex (SnF ₂ (OEP)), protoporphyrin-tin fluoride complex (SnF ₂ (Etio I)), and octaethylporphyrin-platinum chloride complex (PtCl ₂ OEP).

-10-基)苯基]-4，6-二苯基-1，3，5-三嗪(簡稱：PXZ-TRZ)、3-[4- (5-苯基-5，10-二氫啡

-10-基)苯基]-4，5-二苯基-1，2，4-三唑(簡稱：PPZ-3TPT)、3-(9，9-二甲基-9H-吖啶-10-基)-9H-氧雜蒽-9-酮(簡稱：ACRXTN)、雙[4-(9，9-二甲基-9，10-二氫吖啶)苯基]碸(簡稱：DMAC-DPS)、10-苯基-10H，10’H-螺[吖啶-9，9’-蒽]-10’-酮(簡稱：ACRSA)、4-(9’-苯基-3，3’-聯-9H-咔唑-9-基)苯并呋喃并[3，2-d]嘧啶(簡稱：4PCCzBfpm)、4-[4-(9’-苯基-3,3’-聯-9H-咔唑-9-基)苯基]苯并呋喃并[3,2-d]嘧啶(簡稱：4PCCzPBfpm)、9-[3-(4,6-二苯基-1,3,5-三嗪-2-基)苯基]-9’-苯基-2,3’-聯-9H-咔唑(簡稱：mPCCzPTzn-02)等。該雜環化合物具有富π電子雜芳環及缺π電子雜芳環，因此電子傳輸性及電洞傳輸性高，所以是較佳的。尤其是，在具有缺π電子雜芳環的骨架中，吡啶骨架、二嗪骨架(嘧啶骨架、吡嗪骨架、嗒

骨架)及三嗪骨架穩定且可靠性良好，所以是較佳的。尤其是，苯并呋喃并嘧啶骨架、苯并噻吩并嘧啶骨架、苯并呋喃并吡嗪骨架、苯并噻吩并吡嗪骨架的受體性高且可靠性良好，所以是較佳的。另外，在具有富π電子雜芳環的骨架中，吖啶骨架、啡

骨架、啡噻

骨架、呋喃骨架、噻吩骨架及吡咯骨架穩定且可靠性良好，所以較佳為具有上述骨架中的至少一個。另外，作為呋喃骨架較佳為使用二苯并呋喃骨架，作為噻吩骨架較佳為使用二苯并噻吩骨架。作為吡咯骨架，特別較佳為使用吲哚骨架、咔唑骨架，聯咔唑骨架、3-(9-苯基-9H-咔唑-3-基)-9H-咔唑骨架。另外，在富π電子雜芳環和缺π電子雜芳環直接鍵合的物質中，富π電子雜芳環的施體性和缺π電子雜芳環的受體性都強，單重激發態與三重激發態的能階之差變小，所以是尤其較佳的。另外，也可以使用鍵合有如氰基等拉電子基團的芳香環代替缺π電子雜芳環。 In addition, as a TADF material composed of one material, a heterocyclic compound having one or both of a π-electron-rich skeleton and a π-electron-deficient skeleton can also be used. Specifically, 2-(biphenyl-4-yl)-4,6-bis(12-phenylindolo[2,3-a]carbazole-11-yl)-1,3,5-triazine (abbreviated as: PIC-TRZ), 2-{4-[3-(N-phenyl-9H-carbazole-3-yl)-9H-carbazole-9-yl]phenyl}-4,6-diphenyl-1,3,5-triazine (abbreviated as: PCCzPTzn), 2-[4-(10H-phenylindolo[2,3-a]carbazole-11-yl)-1,3,5-triazine (abbreviated as: PCCzPTzn),

-10-yl)phenyl]-4,6-diphenyl-1,3,5-triazine (abbreviated as: PXZ-TRZ), 3-[4-(5-phenyl-5,10-dihydrophenoxy)phenyl]-

-10-yl)phenyl]-4,5-diphenyl-1,2,4-triazole (abbreviated as PPZ-3TPT), 3-(9,9-dimethyl-9H-acridin-10-yl)-9H-oxanthracen-9-one (abbreviated as ACRXTN), bis[4-(9,9-dimethyl-9,10-dihydroacridine)phenyl]sulfone (abbreviated as DMAC-DPS), 10-phenyl-10H,10'H-spiro[acridine-9,9'-anthracen]-10'-one (abbreviated as ACRSA), 4-(9'-phenyl 4-[4-(9'-phenyl-3,3'-bi-9H-carbazole-9-yl)phenyl]benzofurano[3,2-d]pyrimidine (abbreviated as 4PCCzPBfpm), 9-[3-(4,6-diphenyl-1,3,5-triazine-2-yl)phenyl]-9'-phenyl-2,3'-bi-9H-carbazole (abbreviated as mPCCzPTzn-02), etc. The heterocyclic compound has a π-electron-rich heteroaromatic ring and a π-electron-deficient heteroaromatic ring, and thus has high electron and hole transport properties, and is therefore preferred. In particular, among the skeletons having a π-electron-deficient heteroaromatic ring, a pyridine skeleton, a diazine skeleton (pyrimidine skeleton, pyrazine skeleton,

The benzofuranopyrimidine skeleton, benzothienopyrimidine skeleton, benzofuranopyrazine skeleton, and benzothienopyrazine skeleton are preferred because they are stable and reliable. In particular, the benzofuranopyrimidine skeleton, benzothienopyrazine skeleton, and benzothienopyrazine skeleton are preferred because they have high acceptor properties and good reliability. In addition, among the skeletons having π-electron-rich heteroaromatic rings, the acridine skeleton, the phenanthridine skeleton, and the benzothienopyrazine skeleton are preferred because they have high acceptor properties and good reliability.

Skeleton, Morphothiocyanate

Skeletons, furan skeletons, thiophene skeletons and pyrrole skeletons are stable and have good reliability, so it is better to have at least one of the above skeletons. In addition, as the furan skeleton, it is better to use a dibenzofuran skeleton, and as the thiophene skeleton, it is better to use a dibenzothiophene skeleton. As the pyrrole skeleton, it is particularly better to use an indole skeleton, a carbazole skeleton, a bicarbazole skeleton, and a 3-(9-phenyl-9H-carbazole-3-yl)-9H-carbazole skeleton. In addition, in the material in which the π-electron-rich heteroaromatic ring and the π-electron-deficient heteroaromatic ring are directly bonded, the donor property of the π-electron-rich heteroaromatic ring and the acceptor property of the π-electron-deficient heteroaromatic ring are strong, and the difference in energy levels between the singlet excited state and the triplet excited state becomes smaller, so it is particularly better. Alternatively, an aromatic ring bonded with an electron-withdrawing group such as a cyano group may be used instead of a π-electron-deficient heteroaromatic ring.

[Chemical formula 29]

When compound 133 does not have the function of converting triplet excitation energy into luminescence, the combination of compound 131 and compound 133 is preferably a combination that forms an excited complex with each other, but there is no particular limitation. Preferably, one has the function of transporting electrons and the other has the function of transporting holes.

二唑衍生物、三唑衍生物、苯并咪唑衍生物、喹

啉衍生物、二苯并喹

啉衍生物、二苯并噻吩衍生物、二苯并呋喃衍生物、嘧啶衍生物、三嗪衍生物、吡啶衍生物、聯吡啶衍生物、啡啉衍生物等。作為其他例子，可以舉出芳香胺 或咔唑衍生物等。 As compound 131, in addition to zinc and aluminum metal complexes, other examples include

Oxadiazole derivatives, triazole derivatives, benzimidazole derivatives, quinone

Phosphine derivatives, dibenzoquinoline

In some embodiments, the present invention relates to phenanthene derivatives, dibenzothiophene derivatives, dibenzofuran derivatives, pyrimidine derivatives, triazine derivatives, pyridine derivatives, bipyridine derivatives, phenanthene derivatives, etc. Other examples include aromatic amines and carbazole derivatives.

In addition, for example, the following hole-transporting materials and electron-transporting materials can be used.

As the hole transport material, a material having higher hole transport than electron transport can be used, preferably a material having a hole mobility of 1×10 ^-6 cm ² /Vs or more. Specifically, aromatic amines, carbazole derivatives, aromatic hydrocarbons, stilbene derivatives, etc. can be used. The hole transport material may also be a polymer compound.

Examples of materials having high hole transport properties include aromatic amine compounds such as N,N'-di(p-tolyl)-N,N'-diphenyl-p-phenylenediamine (DTDPPA), 4,4'-bis[N-(4-diphenylaminophenyl)-N-anilino]biphenyl (DPAB), N,N'-bis{4-[bis(3-methylphenyl)amino]phenyl}-N,N'-diphenyl-(1,1'-biphenyl)-4,4'-diamine (DNTPD), and 1,3,5-tris[N-(4-diphenylaminophenyl)-N-anilino]benzene (DPA3B).

In addition, specific examples of carbazole derivatives include 3-[N-(4-diphenylaminophenyl)-N-anilino]-9-phenylcarbazole (abbreviated as PCzDPA1), 3,6-bis[N-(4-diphenylaminophenyl)-N-anilino]-9-phenylcarbazole (abbreviated as PCzDPA2), 3,6-bis[N-(4-diphenylaminophenyl)-N-(1-naphthyl)amino]-9-phenylcarbazole (abbreviated as PCzDPA2). : PCzTPN2), 3-[N-(9-phenylcarbazole-3-yl)-N-anilino]-9-phenylcarbazole (abbreviated as: PCzPCA1), 3,6-bis[N-(9-phenylcarbazole-3-yl)-N-anilino]-9-phenylcarbazole (abbreviated as: PCzPCA2), 3-[N-(1-naphthyl)-N-(9-phenylcarbazole-3-yl)amino]-9-phenylcarbazole (abbreviated as: PCzPCN1), etc.

In addition, examples of carbazole derivatives include 4,4'-di(N-carbazolyl)biphenyl (abbreviated as CBP), 1,3,5-tris[4-(N-carbazolyl)phenyl]benzene (abbreviated as TCPB), 9-[4-(10-phenyl-9-anthracenyl)phenyl]-9H-carbazole (abbreviated as CzPA), and 1,4-bis[4-(N-carbazolyl)phenyl]-2,3,5,6-tetraphenylbenzene.

Examples of the aromatic hydrocarbon include 2-tert-butyl-9,10-di(2-naphthyl)anthracene (abbreviation: t-BuDNA), 2-tert-butyl-9,10-di(1-naphthyl)anthracene, 9,10-bis(3,5-diphenylphenyl)anthracene (abbreviation: DPPA), 2-tert-butyl-9,10-bis(4-phenylphenyl)anthracene (abbreviation: t-BuDBA), 9,10-di(2-naphthyl)anthracene (abbreviation: DNA), 9,10-diphenylanthracene (abbreviation: DPAnth), 2-tert-butylanthracene (abbreviation: t-BuAnth), and 9,10-bis(4-methyl-1-naphthyl)anthracene (abbreviation: DMNA). , 2-tert-butyl-9,10-bis[2-(1-naphthyl)phenyl]anthracene, 9,10-bis[2-(1-naphthyl)phenyl]anthracene, 2,3,6,7-tetramethyl-9,10-di(1-naphthyl)anthracene, 2,3,6,7-tetramethyl-9,10-di(2-naphthyl)anthracene, 9,9'-bianthracene, 10,10'-diphenyl-9,9'-bianthracene, 10,10'-bis(2-phenylphenyl)-9,9'-bianthracene, 10,10'-bis[(2,3,4,5,6-pentaphenyl)phenyl]-9,9'-bianthracene, anthracene, fused tetraphenyl, rubrene, perylene, 2,5,8,11-tetra(tert-butyl)perylene, etc. In addition, fused pentadiene, coronene, etc. can also be used. Thus, it is more preferable to use an aromatic hydrocarbon having a hole mobility of 1×10 ^-6 cm ² /Vs or more and having 14 to 42 carbon atoms.

Note that the aromatic hydrocarbon may also have a vinyl skeleton. Examples of aromatic hydrocarbons having a vinyl group include 4,4'-bis(2,2-diphenylvinyl)biphenyl (abbreviation: DPVBi) and 9,10-bis[4-(2,2-diphenylvinyl)phenyl]anthracene (abbreviation: DPVPA).

In addition, polymer compounds such as poly(N-vinylcarbazole) (abbreviation: PVK), poly(4-vinyltriphenylamine) (abbreviation: PVTPA), poly[N-(4-{N’-[4-(4-diphenylamino)phenyl]phenyl-N’-phenylamino}phenyl)methacrylamide] (abbreviation: PTPDMA), and poly[N,N’-bis(4-butylphenyl)-N,N’-bis(phenyl)benzidine] (abbreviation: Poly-TPD) can also be used.

In addition, as a material with high hole transport properties, for example, 4,4'-bis[N-(1-naphthyl)-N-anilino]biphenyl (abbreviated as NPB or α-NPD), N,N'-bis(3-methylphenyl)-N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine (abbreviated as TPD), 4,4',4''-tri(carbazol-9-yl)triphenylamine (abbreviated as TCTA), 4,4',4''-tri[N-(1-naphthyl)- N-anilino]triphenylamine (abbreviated as: 1'-TNATA), 4,4',4''-tris(N,N-diphenylamino)triphenylamine (abbreviated as: TDATA), 4,4',4''-tris[N-(3-methylphenyl)-N-anilino]triphenylamine (abbreviated as: MTDATA), 4,4'-bis[N-(spiro-9,9'-bifluoren-2-yl)-N-anilino]biphenyl (abbreviated as: BSPB), 4-phenyl-4'-(9-phenylfluoren-9-yl)- )triphenylamine (abbreviated as: BPAFLP), 4-phenyl-3'-(9-phenylfluoren-9-yl)triphenylamine (abbreviated as: mBPAFLP), N-(9,9-dimethyl-9H-fluoren-2-yl)-N-{(9,9-dimethyl-2-[N'-phenyl-N'-(9,9-dimethyl-9H-fluoren-2-yl)amino]-9H-fluoren-7-yl}phenylamine (abbreviated as: DFLADFL), N-(9,9-dimethyl-2-diphenylamino-9 H-fluoren-7-yl) diphenylamine (abbreviated as: DPNF), 2-[N-(4-diphenylaminophenyl)-N-anilino]spiro-9,9'-bifluoren-7-yl (abbreviated as: DPASF), 4-phenyl-4'-(9-phenyl-9H-carbazole-3-yl)triphenylamine (abbreviated as: PCBA1BP), 4,4'-diphenyl-4''-(9-phenyl-9H-carbazole-3-yl)triphenylamine (abbreviated as: PCBBi1BP), 4-(1-naphthyl)-4' -(9-phenyl-9H-carbazole-3-yl)triphenylamine (abbreviated as: PCBANB), 4,4'-di(1-naphthyl)-4''-(9-phenyl-9H-carbazole-3-yl)triphenylamine (abbreviated as: PCBNBB), 4-phenyldiphenyl-(9-phenyl-9H-carbazole-3-yl)amine (abbreviated as: PCA1BP), N,N'-bis(9-phenylcarbazole-3-yl)-N,N'-diphenylbenzene-1,3-diamine (abbreviated as: PCA2B) 、N，N'，N''-triphenyl-N，N'，N''-tri(9-phenylcarbazole-3-yl)benzene-1，3，5-triamine (abbreviated as PCA3B), N-(4-biphenyl)-N-(9,9-dimethyl-9H-fluoren-2-yl)-9-phenyl-9H-carbazole-3-amine (abbreviated as PCBiF), N-(1，1'-biphenyl-4-yl)-N-[4-(9-phenyl-9H-carbazole-3-yl)phenyl]-9，9-dimethyl-9 H-fluoren-2-amine (abbreviated as: PCBBiF), 9,9-dimethyl-N-phenyl-N-[4-(9-phenyl-9H-carbazole-3-yl)phenyl]fluoren-2-amine (abbreviated as: PCBAF), N-phenyl-N-[4-(9-phenyl-9H-carbazole-3-yl)phenyl]spiro-9,9'-bifluoren-2-amine (abbreviated as: PCBASF), 2-[N-(9-phenylcarbazole-3-yl)-N-anilino]spiro-9,9'-bifluoren-2-amine (abbreviated as: : PCASF), 2,7-bis[N-(4-diphenylaminophenyl)-N-anilino]spiro-9,9'-bifluorene (abbreviated as: DPA2SF), N-[4-(9H-carbazole-9-yl)phenyl]-N-(4-phenyl)phenylaniline (abbreviated as: YGA1BP), N,N'-bis[4-(carbazole-9-yl)phenyl]-N,N'-diphenyl-9,9-dimethylfluorene-2,7-diamine (abbreviated as: YGA2F) and other aromatic amine compounds. In addition, 3-[4-(1-naphthyl)-phenyl]-9-phenyl-9H-carbazole (abbreviated as PCPN), 3-[4-(9-phenanthrenyl)-phenyl]-9-phenyl-9H-carbazole (abbreviated as PCPPn), 3,3'-bis(9-phenyl-9H-carbazole) (abbreviated as PCCP), 1,3-bis(N-carbazolyl)benzene (abbreviated as mCP), 3,6-bis(3,5-diphenylphenyl)-9-phenylcarbazole (abbreviated as CzTP), 4-{(3-[3-(9-phenyl-9H-fluoren-9-yl)phenyl]phenyl}dibenzofuran (abbreviated as mmDBFFLBi-II), 4,4',4''-(benzene-1,3,5-triyl)tris(dibenzofuran) (abbreviated as mCP), 3,6-bis(3,5-diphenylphenyl)-9-phenylcarbazole (abbreviated as CzTP), 4-{(3-[3-(9-phenyl-9H-fluoren-9-yl)phenyl]phenyl}dibenzofuran (abbreviated as mmDBFFLBi-II), 3,3'-bis(9-phenyl-9H-triyl)benzene (abbreviated as mCP), 3,6-bis(3,5-diphenylphenyl)-9-phenylcarbazole ...N-carbazolyl)benzene (abbreviated as mCP), 3,6-bis(N-carbazolyl)benzene (abbreviated as mCP), abbreviation: DBF3P-II), 1,3,5-tris(dibenzothiophene-4-yl)benzene (abbreviation: DBT3P-II), 2,8-diphenyl-4-[4-(9-phenyl-9H-fluoren-9-yl)phenyl]dibenzothiophene (abbreviation: DBTFLP-III), 4-[4-(9-phenyl-9H-fluoren-9-yl)phenyl]-6-phenyldibenzothiophene (abbreviation: DBTFLP-IV), 4-[3-(triphenyl-2-yl)phenyl]dibenzothiophene (abbreviation: mDBTPTp-II), etc., amine compounds, carbazole compounds, thiophene compounds, furan compounds, fluoren-4-yl compounds, triphenyl compounds, phenanthrene compounds, etc. The substances described here are mainly amine compounds with a hole mobility of 1×10 ^-6 cm ² /Vs or more. However, any substance other than the above substances may be used as long as it has a hole-transmitting property higher than an electron-transmitting property.

唑配體或噻唑配體的金屬錯合物、

二唑衍生物、三唑衍生物、啡啉衍生物、吡啶衍生物、聯吡啶衍生物、嘧啶衍生物等。 As the electron-transmitting material, a material having a higher electron-transmitting property than a hole-transmitting property can be used, and preferably a material having an electron mobility of 1×10 ^-6 cm ² /Vs or more can be used. As the material that easily receives electrons (material having electron-transmitting property), a π-electron-deficient heteroaromatic compound such as a nitrogen-containing heteroaromatic compound or a metal complex can be used. As specific examples, quinoline ligands, benzoquinoline ligands,

A metal complex of an azole ligand or a thiazole ligand,

Oxadiazole derivatives, triazole derivatives, phenanthroline derivatives, pyridine derivatives, bipyridine derivatives, pyrimidine derivatives and the like.

唑基)苯酚]鋅(II)(簡稱：ZnPBO)、雙[2-(2-苯并噻唑基)苯酚]鋅(II)(簡稱：ZnBTZ)等具有

唑基類、噻唑類配體的金屬錯合物等。再者，除了金屬錯合物以外，還可以使用2-(4-聯苯基)-5-(4-三級丁基苯基)-1，3，4-

二唑(簡稱：PBD)、1，3-雙[5-(對三級基丁苯基)-1，3，4-

二唑-2-基]苯(簡稱：OXD-7)、9-[4-(5-苯基-1，3，4-

二唑-2-基)苯基]-9H-咔唑(簡稱：CO11)、3-(4-聯苯基)-4-苯基-5-(4-三級丁基苯基)-1，2，4-三唑(簡稱：TAZ)、2，2’，2’’-(1，3，5-苯三基)三(1-苯基-1H-苯并咪唑)(簡稱：TPBI)、2-[3-(二苯并噻吩-4-基)苯基]-1-苯基-1H-苯并咪唑(簡稱：mDBTBIm-II)、紅啡啉(簡稱：BPhen)、2，9-雙(萘-2-基)-4，7-二苯基-1，10-啡啉(簡稱：NBPhen)、浴銅靈(簡稱：BCP)等雜環化合物；2-[3-(二苯并噻吩-4-基)苯基]二苯并[f，h]喹

啉(簡稱：2mDBTPDBq-II)、2-[3’-(二苯并噻吩-4-基)聯苯-3-基]二苯并[f，h]喹

啉(簡稱：2mDBTBPDBq-II)、2-[3’-(9H-咔唑-9-基)聯苯-3-基]二苯并[f，h]喹

啉(簡稱：2mCzBPDBq)、2-[4-(3，6-二苯基-9H-咔唑-9-基)苯基]二苯并[f，h]喹

啉(簡稱：2CzPDBq-III)，7-[3-(二苯并噻吩-4-基)苯基]二苯并[f，h]喹

啉(簡稱：7mDBTPDBq-II)、6-[3-(二苯并噻吩-4-基)苯基]二苯并[f，h]喹

啉(簡稱：6mDBTPDBq-II)、4，6-雙[3-(菲-9-基)苯基]嘧啶(簡稱：4,6mPnP2Pm)、4，6-雙[3-(4-二苯并噻吩基)苯基]嘧啶(簡稱：4,6mDBTP2Pm-II)、4，6-雙[3-(9H-咔唑-9-基)苯基]嘧啶(簡稱：4,6mCzP2Pm)等具有二嗪骨架的雜環化合物；2-{4-[3-(N-苯基-9H-咔唑-3-基)-9H-咔唑-9-基]苯基}-4,6-二苯基 -1,3,5-三嗪(簡稱：PCCzPTzn)等具有三嗪骨架的雜環化合物；3，5-雙[3-(9H-咔唑-9-基)苯基]吡啶(簡稱：35DCzPPy)、1，3，5-三[3-(3-吡啶基)苯基]苯(簡稱：TmPyPB)等具有吡啶骨架的雜環化合物；4，4’-雙(5-甲基苯并

唑基-2-基)二苯乙烯(簡稱：BzOs)等雜芳香化合物。另外，還可以使用高分子化合物諸如聚(2,5-吡啶二基)(簡稱：PPy)、聚[(9,9-二己基茀-2,7-二基)-共-(吡啶-3,5-二基)](簡稱：PF-Py)、聚[(9,9-二辛基茀-2,7-二基)-共-(2,2’-聯吡啶-6,6’-二基)](簡稱：PF-BPy)。在此所述的物質主要是電子移動率為1×10^-6cm²/Vs以上的物質。注意，只要是電子傳輸性高於電洞傳輸性的物質，就可以使用上述物質以外的物質。 For example, metal complexes having a quinoline skeleton or a benzoquinoline skeleton such as tris(8-hydroxyquinolinato)aluminum(III) (abbreviated as: Alq), tris(4-methyl-8-hydroxyquinolinato)aluminum(III) (abbreviated as: Almq ₃ ), bis(10-hydroxybenzo[h]quinolinato)borate(II) (abbreviated as: BeBq ₂ ), bis(2-methyl-8-hydroxyquinolinato)(4-phenylphenol)aluminum(III) (abbreviated as: BAlq), bis(8-hydroxyquinolinato)zinc(II) (abbreviated as: Znq) and the like can be used. In addition, bis[2-(2-benzo[h]quinolinato)aluminum(III) (abbreviated as: BeBq 2 ) can be used.

Bis[2-(2-benzothiazolyl)phenol]zinc(II) (abbreviated as ZnPBO), bis[2-(2-benzothiazolyl)phenol]zinc(II) (abbreviated as ZnBTZ) etc.

In addition to metal complexes, 2-(4-biphenyl)-5-(4-tert-butylphenyl)-1,3,4-

PBD), 1,3-bis[5-(p-tert-butylphenyl)-1,3,4-

oxadiazole-2-yl]benzene (abbreviated as OXD-7), 9-[4-(5-phenyl-1,3,4-

heterocyclic compounds such as 2-[(1-(dibenzothiophene-4-yl)phenyl]-1-phenyl-1H-benzimidazole (abbreviated as: mDBTBIm-II), 2-[(1-(dibenzothiophene-2-yl)phenyl)-9H-carbazole (abbreviated as: CO11), 3-(4-biphenyl)-4-phenyl-5-(4-tert-butylphenyl)-1,2,4-triazole (abbreviated as: TAZ), 2,2',2''-(1,3,5-benzenetriyl)tris(1-phenyl-1H-benzimidazole) (abbreviated as: TPBI), 2-[3-(dibenzothiophene-4-yl)phenyl]-1-phenyl-1H-benzimidazole (abbreviated as: mDBTBIm-II), 2-[(1-(dibenzothiophene-2-yl)phenyl)-1-phenyl-1H-benzimidazole) (abbreviated as: mDBTBIm-II), 2,9-bis(naphthalene-2-yl)-4,7-diphenyl-1,10-phenanthroline (abbreviated as: NBPhen), and bathocophine (abbreviated as: BCP); 2-[3-(dibenzothiophene-4-yl)phenyl]dibenzo[f,h]quinoline

quinoline (abbreviated as: 2mDBTPDBq-II), 2-[3'-(dibenzothiophene-4-yl)biphenyl-3-yl]dibenzo[f,h]quinoline

quinoline (abbreviated as: 2mDBTBPDBq-II), 2-[3'-(9H-carbazole-9-yl)biphenyl-3-yl]dibenzo[f,h]quinoline

quinoline (abbreviated as: 2mCzBPDBq), 2-[4-(3,6-diphenyl-9H-carbazole-9-yl)phenyl]dibenzo[f,h]quinoline

quinoline (abbreviated as: 2CzPDBq-III), 7-[3-(dibenzothiophen-4-yl)phenyl]dibenzo[f,h]quinoline

quinoline (abbreviated as: 7mDBTPDBq-II), 6-[3-(dibenzothiophen-4-yl)phenyl]dibenzo[f,h]quinoline

Heterocyclic compounds having a diazine skeleton, such as 4,6-bis[3-(phenanthrene-9-yl)phenyl]pyrimidine (abbreviated as 4,6mPnP2Pm), 4,6-bis[3-(4-dibenzothienyl)phenyl]pyrimidine (abbreviated as 4,6mDBTP2Pm-II), 4,6-bis[3-(9H-carbazol-9-yl)phenyl]pyrimidine (abbreviated as 4,6mCzP2Pm); 2-{4-[3-(N-phenyl- Heterocyclic compounds with a triazine skeleton such as 3,5-bis[3-(9H-carbazole-3-yl)-9H-carbazole-9-yl]phenyl}-4,6-diphenyl-1,3,5-triazine (abbreviated as PCCzPTzn); Heterocyclic compounds with a pyridine skeleton such as 3,5-bis[3-(9H-carbazole-9-yl)phenyl]pyridine (abbreviated as 35DCzPPy) and 1,3,5-tris[3-(3-pyridyl)phenyl]benzene (abbreviated as TmPyPB); 4,4'-bis(5-methylbenzoic acid)

Miscellaneous aromatic compounds such as poly(2,5-pyridinediyl) (abbreviated as PPy), poly[(9,9-dihexylfluorene-2,7-diyl)-co-(pyridine-3,5-diyl)] (abbreviated as PF-Py), and poly[(9,9-dioctylfluorene-2,7-diyl)-co-(2,2'-bipyridine-6,6'-diyl)] (abbreviated as PF-BPy) can also be used. The substances described here are mainly substances having an electron mobility of 1×10 ^-6 cm ² /Vs or more. Note that substances other than the above substances may be used as long as the electron transport property is higher than the hole transport property.

Compound 133 is preferably a material that can form an excited complex with compound 131. Specifically, the hole-transmitting material and the electron-transmitting material shown above can be used. At this time, compound 131 and compound 133, as well as compound 132 (fluorescent material) are selected in such a way that the luminescence peak of the excited complex formed by compound 131 and compound 133 overlaps with the absorption band on the longest wavelength side (low energy side) of compound 132 (fluorescent material). Thus, a light-emitting element with significantly improved luminescence efficiency can be achieved.

As compound 133 and/or compound 136, a phosphorescent material can be used. As the phosphorescent material, iridium, rhodium, platinum-based organic metal complexes or metal complexes can be cited. In addition, platinum complexes or organic iridium complexes having porphyrin ligands can be cited, and in particular, for example, organic iridium complexes such as iridium-based ortho-metal complexes are preferably used. As ortho-metallated ligands, 4H-triazole ligands, 1H-triazole ligands, imidazole ligands, pyridine ligands, pyrimidine ligands, pyrazine ligands or isoquinoline ligands can be cited. At this time, compound 133 (phosphorescent material) has an absorption band with a triple MLCT (metal to ligand charge transfer) transition. In addition, it is preferred to select compound 133 and compound 132 (fluorescent material) in such a way that the luminescence peak of compound 133 overlaps with the absorption band on the longest wavelength side (low energy side) of compound 132 (fluorescent material). In this way, a light-emitting element with significantly improved luminescence efficiency can be achieved. In addition, even if compound 133 is a phosphorescent material, it can form an excited state complex with compound 131. When the excited state complex is formed, the phosphorescent material does not need to emit light at room temperature, and it only needs to be able to emit light at room temperature when the excited state complex is formed. At this time, for example, tris[2-(1H-pyrazol-1-yl-κN ² )phenyl-κC]iridium (III) (abbreviated as: Ir(ppz) ₃ ) and the like can be used as a phosphorescent material. Furthermore, it is preferred that compound 132 and compound 136 be selected so that the emission peak of compound 132 overlaps with the absorption band on the longest wavelength side (low energy side) of compound 136. In this way, a multicolor light-emitting element with good light-emitting efficiency can be produced.

Examples of substances having a luminescence peak in the blue or green wavelength region include tris{2-[5-(2-methylphenyl)-4-(2,6-dimethylphenyl)-4H-1,2,4-triazol-3-yl-κN ² ]phenyl-κC}iridium(III) (abbreviated as Ir(mpptz-dmp) ₃ ), tris(5-methyl-3,4-diphenyl-4H-1,2,4-triazole)iridium(III) (abbreviated as Ir(Mptz) ₃ ), tris[4-(3-biphenyl)-5-isopropyl-3-phenyl-4H-1,2,4-triazole]iridium(III) (abbreviated as Ir(iPrptz-3b) ₃ ), tris[3-(5-biphenyl)-5-isopropyl-4-phenyl-4H-1,2,4-triazole] iridium(III) (abbreviated as Ir(iPr5btz) ₃ ), tris[3-methyl-1-(2-methylphenyl)-5-phenyl-1H-1,2,4-triazole] iridium(III) (abbreviated as Ir(Mptz1-mp) ₃ ), tris(1-methyl-5-phenyl-3-propyl-1H-1,2,4-triazole) iridium(III) (abbreviated as Ir(Prptz1-Me) ₃ ) and other organometallic iridium complexes having a 1H-triazole skeleton; fac-tris[1-(2,6-diisopropylphenyl)-2-phenyl-1H-imidazole] iridium(III) (abbreviated as: Ir(iPrpmi) ₃ ), tris[3-(2,6-dimethylphenyl)-7-methylimidazo[1,2-f]phenanthridinato] iridium(III) (abbreviated as: Ir(dmpimpt-Me) ₃ ) and other organometallic iridium complexes having an imidazole skeleton; and bis[2-(4',6'-difluorophenyl)pyridinium-N,C ^2' ] iridium(III)tetrakis(1-pyrazolyl)borate (abbreviated as: FIr6), bis[2-(4',6'-difluorophenyl)pyridinium-N,C ^2' ] iridium (III) picolinate (abbreviation: FIrpic), bis{2-[3',5'-bis(trifluoromethyl)phenyl]pyridinium-N,C ^2' } iridium (III) picolinate (abbreviation: Ir(CF ₃ ppy) ₂ (pic)), bis[2-(4',6'-difluorophenyl)pyridinium-N,C ^2' ]iridium (III) acetylacetone (abbreviation: FIr(acac)), etc., which have phenylpyridine derivatives having electron-withdrawing groups as ligands. Among the above materials, organometallic iridium complexes having nitrogen-containing five-membered heterocyclic skeletons such as 4H-triazole skeletons, 1H-triazole skeletons and imidazole skeletons are particularly preferred because of their high triplet excitation energy, high reliability and high luminescence efficiency.

唑-N，C^2’)銥(III)乙醯丙酮(簡稱：Ir(dpo)₂(acac))、雙{2-[4’-(全氟苯基)苯基]吡啶-N，C^2’}銥(III)乙醯丙酮(簡稱：Ir(p-PF-ph)₂(acac))、雙(2-苯基苯并噻唑-N，C^2’)銥(III)乙醯丙酮(簡稱：Ir(bt)₂(acac))等有機金屬銥錯合物；三(乙醯丙酮根)(單啡啉)鋱(III)(簡稱：Tb(acac)₃(Phen))等稀土金屬錯合物。在上述材料中，由於具有嘧啶骨架的有機金屬銥錯合物具有非常高的可靠性及發光效率，所以是尤其較佳的。 Examples of substances having a luminescence peak in the green or yellow wavelength region include tris(4-methyl-6-phenylpyrimidinyl) iridium(III) (abbreviation: Ir(mppm) ₃ ), tris(4-tert-butyl-6-phenylpyrimidinyl) iridium(III) (abbreviation: Ir(tBuppm) ₃ ), (acetylacetonato)bis(6-methyl-4-phenylpyrimidinyl) iridium(III) (abbreviation: Ir(mppm) ₂ (acac)), (acetylacetonato)bis(6-tert-butyl-4-phenylpyrimidinyl) iridium(III) (abbreviation: Ir(tBuppm) ₂ (acac)), (acetylacetonato)bis(4-(2-norbornyl)-6-phenylpyrimidinyl) iridium(III) (abbreviation: Ir(nbppm) ₂ (acac)), (acetylacetonato)bis[5-methyl-6-(2-methylphenyl)-4-phenylpyrimidinyl] iridium(III) (abbreviated as Ir(mpmppm) ₂ (acac)), (acetylacetonato)bis{(4,6-dimethyl-2-[6-(2,6-dimethylphenyl)-4-pyrimidinyl-κN ³ ]phenyl-κC} iridium(III) (abbreviated as Ir(dmppm-dmp) ₂ (acac)), (acetylacetonato)bis(4,6-diphenylpyrimidinyl) iridium(III) (abbreviated as Ir(dppm) ₂ (acac)), etc.; (acetylacetonato)bis(3,5-dimethyl-2-phenylpyrazine) iridium(III) (abbreviated as Ir(mppr-Me) ₂ (acac)), (acetylacetonato)bis(5-isopropyl-3-methyl-2-phenylpyrazine) iridium(III) (abbreviated as Ir(mppr-iPr) ₂ (acac)), etc.; tris(2-phenylpyridinium-N,C ² ') iridium(III) (abbreviated as Ir(ppy) ₃ ), bis(2-phenylpyridinium-N,C ^2' ) iridium(III) acetylacetonate (abbreviated as Ir(ppy) ₂ (acac)), bis(benzo[h]quinoline) iridium(III) acetylacetonate (abbreviated as Ir(bzq) ₂ (acac)), tris(benzo[h]quinoline) iridium(III) (abbreviated as Ir(bzq) ₃ ), tris(2-phenylquinoline-N,C ^{2 '} ) iridium (III) (abbreviated as Ir(pq) ₃ ), bis(2-phenylquinoline-N,C ^2' ) iridium (III) acetylacetonate (abbreviated as Ir(pq) ₂ (acac)) and other organometallic iridium complexes having a pyridine skeleton; bis(2,4-diphenyl-1,3-

Organometallic iridium complexes such as (2-(4-(2-phenylbenzothiazole-N, C ^{2 '} ) iridium (III) acetylacetonate (abbreviated as Ir(dpo) ₂ (acac)), (2-(4-(2-phenylbenzothiazole-N, C 2') iridium (III) acetylacetonate (abbreviated as Ir(p-PF-ph) ₂ (acac)), (2-(2-phenylbenzothiazole-N, C ^2' ) iridium (III) acetylacetonate (abbreviated as Ir(bt) ₂ (acac)); and (3-(2-(2-phenylbenzothiazole-N, C 2') iridium (III) acetylacetonate (abbreviated as Tb(acac) ₃ (Phen)). Among the above materials, organometallic iridium complexes having a pyrimidine skeleton are particularly preferred because they have very high reliability and luminescence efficiency.

啉]合銥(III)(簡稱：Ir(Fdpq)₂(acac))、雙{4,6-二甲基-2-[5-(2,6-二甲基苯基)-3-(3,5-二甲基苯基)-2-吡嗪基-κN]苯基-κC}(2,2’,6,6’-四甲基-3,5-庚二酮-κ²0,0’)銥(III)(簡稱：Ir(dmdppr-dmp)₂(dpm))等具有吡 嗪骨架的有機金屬銥錯合物；三(1-苯基異喹啉-N，C^2’)銥(III)(簡稱：Ir(piq)₃)、雙(1-苯基異喹啉-N，C^2’)銥(III)乙醯丙酮(簡稱：Ir(piq)₂(acac))等具有吡啶骨架的有機金屬銥錯合物；2，3，7，8，12，13，17，18-八乙基-21H，23H-卟啉鉑(II)(簡稱：Pt0EP)等鉑錯合物；以及三(1，3-二苯基-1，3-丙二酮(propanedionato))(單啡啉)銪(III)(簡稱：Eu(DBM)₃(Phen))、三[1-(2-噻吩甲醯基)-3，3，3-三氟丙酮](單啡啉)銪(III)(簡稱：Eu(TTA)₃(Phen))等稀土金屬錯合物。在上述物質中，由於具有嘧啶骨架的有機金屬銥錯合物也具有非常高的可靠性及發光效率，所以是尤其較佳的。另外，具有吡嗪骨架的有機金屬銥錯合物可以獲得色度良好的紅色發光。 In addition, as a substance having a luminescence peak in the yellow or red wavelength region, for example, there can be cited organometallic iridium complexes having a pyrimidine skeleton, such as (diisobutylenemethano)bis[4,6-bis(3-methylphenyl)pyrimidinato]iridium(III) (abbreviated as Ir(5mdppm) ₂ (dibm)), bis[4,6-bis(3-methylphenyl)pyrimidinato](dineopentanoylmethanato)iridium(III) (abbreviated as Ir(5mdppm) ₂ (dpm)), and bis[4,6-di(naphthalene-1-yl)pyrimidinato](dineopentanoylmethanato)iridium(III) (abbreviated as Ir(d1npm) ₂ (dpm)); (acetylacetonato)bis(2,3,5 -triphenylpyrazine) ^iridium (III) (abbreviated as Ir(tppr) ₂ (acac)), bis(2,3,5 ^- triphenylpyrazine) (dipentanoylmethanone) iridium (III) (abbreviated as Ir(tppr) ₂ (dpm)), (acetylacetonate) bis[2,3-bis(4-fluorophenyl)quinoline

Organometallic iridium complexes with pyrazine skeletons, such as tris(1-phenylisoquinoline-N, C 2' ) iridium(III) (abbreviated as Ir(piq) ₃ ), bis(1- _{phenylisoquinoline} -N, ^{C 2 '} ) iridium(III) acetylacetone (abbreviated _as Ir(piq) ₂ (acac)) and other organometallic iridium complexes having a pyridine skeleton; platinum complexes such as 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphyrin platinum (II) (abbreviated as: Pt0EP); and rare earth metal complexes such as tris(1,3-diphenyl-1,3-propanedione)(monomorphous)piperidinium (III) (abbreviated as: Eu(DBM) ₃ (Phen)), tris[1-(2-thienylcarbonyl)-3,3,3-trifluoroacetone](monomorphous)piperidinium (III) (abbreviated as: Eu(TTA) ₃ (Phen)). Among the above substances, organometallic iridium complexes having a pyrimidine skeleton are particularly preferred because they also have very high reliability and luminescence efficiency. In addition, organometallic iridium complexes with a pyrazine skeleton can obtain red luminescence with good chromaticity.

In addition, as a material that can be used as the energy donor, a metal halide calcium-titanium ore material can be cited. The metal halide calcium-titanium ore material can be represented by any one of the following general formulas (g1) to (g3).

(SA)MX ₃ ：(g1)

(LA) ₂ (SA) _n-1 M _n X _3n+1 : (g2)

(PA)(SA) _n-1 M _n X3 _n+1 : (g3)

In the above general formula, M represents a divalent metal ion, and X represents a halogen ion.

Specifically, as the divalent metal ions, divalent cations such as lead and tin are used.

Specifically, as the halogen ions, anions such as chlorine, bromine, iodine, and fluorine are used.

In addition, although n represents an integer of 1 to 10, when n is greater than 10 in the general formula (g2) or the general formula (g3), its properties are similar to those of the metal halide calcium-titanium mineral material represented by the general formula (g1).

Furthermore, LA represents an ammonium ion represented by R ³⁰ -NH ₃ ⁺ .

In the ammonium ion represented by the general formula R ³⁰ -NH ₃ ⁺ , R ³⁰ is: any one of an alkyl group, an aryl group and a heteroaryl group having 2 to 20 carbon atoms; or a group composed of an alkyl group, an aryl group or a heteroaryl group having 2 to 20 carbon atoms and an alkylene group, a vinylene group, an arylene group and a heteroarylene group having 1 to 12 carbon atoms. In the case of the latter, a plurality of alkylene groups, vinylene groups, arylene groups and heteroarylene groups may be linked together, or a plurality of groups of the same type may be used. When a plurality of alkylene groups, vinylene groups, arylene groups and heteroarylene groups are linked together, the total number of alkylene groups, vinylene groups, arylene groups and heteroarylene groups is preferably 35 or less.

SA represents a monovalent metal ion or an ammonium ion represented by R ³¹ -NH ₃ ⁺ , wherein R ³¹ represents an alkyl group having 1 to 6 carbon atoms.

PA represents NH ₃ ⁺ -R ³² -NH ₃ ⁺ , NH ₃ ⁺ -R ³³ -R ³⁴ -R ³⁵ -NH ₃ ⁺ or a part or all of a branched polyethyleneimine containing ammonium cations, and the valence of the part is +2. The charges in the general formula are almost balanced.

Here, the charge of the metal halide calcium-titanium material does not necessarily need to be strictly balanced in all parts of the material according to the above general formula, as long as the material as a whole is kept neutral. Other ions such as already dissociated ammonium ions, already dissociated halogen ions, and impurity ions may exist locally in the material, and sometimes they neutralize the charge. In addition, sometimes the surface of a particle or a film, the grain boundary of a crystal, etc., may not be kept neutral locally, and it is not necessarily necessary to keep all parts neutral.

As (LA) in the general formula (g2), for example, substances represented by the following general formulae (a-1) to (a-11) and (b-1) to (b-6) can be used.

[Chemical formula 30]

(PA) in the above general formula (g3) typically represents a substance represented by any of the following general formulas (c-1), (c-2) and (d) and a part or all of a branched polyethyleneimine containing ammonium cations, and has a +2 charge. These polymers sometimes neutralize charges in a plurality of unit lattices, or sometimes each charge included in two different polymer molecules neutralizes the charge in one unit lattice.

However, in the above general formula, ^R20 represents an alkyl group having 2 to 18 carbon atoms, ^R21 , ^R22 and ^R23 represent hydrogen or an alkyl group having 1 to 18 carbon atoms, and ^R24 represents the following structural formula and general formulas ( ^R24-1 ) to ( ^R24-14 ). ^R25 and ^R26 each independently represent hydrogen or an alkyl group having 1 to 6 carbon atoms. X represents a combination of monomer units A and B represented by any one of the above (d-1) to (d-6), and has a structure including monomer units A and B, the number of monomer units A is u, and the number of monomer units B is v. Note that there is no restriction on the arrangement order of monomer units A and B. m and 1 each independently represent integers from 0 to 12, and t is an integer from 1 to 18. u is an integer from 0 to 17, v is an integer from 1 to 18, and u+v is an integer from 1 to 18.

Note that these descriptions are just examples, and the substances that can be used for (LA) and (PA) are not limited to these.

In a three-dimensionally structured metal halide calcium titanite material having a composition of (SA)MX ₃ represented by the general formula (g1), a regular octahedral structure having a metal atom M at the center and halogen atoms at the six vertices is three-dimensionally arranged in such a way that the halogen atoms at each vertex are used in common to form a skeleton. The regular octahedral structural unit having a halogen atom at each vertex is referred to as a calcium titanite unit. As a structure, there are: a zero-dimensional structure in which the above-mentioned calcium-titanium unit exists alone; a linear structure in which the calcium-titanium unit is connected one-dimensionally by halogen atoms at the vertices; a thin-sheet structure in which the calcium-titanium unit is connected two-dimensionally; and a structure in which the calcium-titanium unit is connected three-dimensionally. In addition, there is: a complex two-dimensional structure formed by stacking a plurality of thin-sheet structures in which the calcium-titanium unit is connected two-dimensionally. In addition, there are more complex structures. In definition, all these structures including the calcium-titanium unit are collectively referred to as metal halide calcium-titanium materials.

The light-emitting layer 130 may also be formed of two or more layers. For example, when the light-emitting layer 130 is formed by stacking a first light-emitting layer and a second light-emitting layer in sequence from the hole transport layer side, a substance having hole transport properties may be used as a main material of the first light-emitting layer, and a substance having electron transport properties may be used as a main material of the second light-emitting layer.

In addition, the light-emitting layer 130 may contain a material (compound 135) other than compound 131, compound 132, and compound 133. In this case, in order to allow compound 131 and compound 133 to efficiently form an excited complex, it is preferred that the HOMO energy level of one of compound 131 and compound 133 is the highest among the materials in the light-emitting layer 130, and the LUMO energy level of the other of compound 131 and compound 132 is the lowest among the materials in the light-emitting layer 130. By adopting this energy level correlation, the reaction of compound 131 and compound 135 to form an excited complex can be suppressed.

For example, when compound 131 has hole transport properties and compound 133 has electron transport properties, it is preferred that the HOMO energy level of compound 131 is higher than the HOMO energy level of compound 133 and the HOMO energy level of compound 135, and the LUMO energy level of compound 133 is lower than the LUMO energy level of compound 131 and the LUMO energy level of compound 135. In this case, the LUMO energy level of compound 135 may be higher or lower than the LUMO energy level of compound 131. In addition, the HOMO energy level of compound 135 may be higher or lower than the HOMO energy level of compound 133.

唑基)苯酚]鋅(II)(簡稱：ZnPBO)、雙[2-(2-苯并噻唑基)苯酚]鋅(II)(簡稱：ZnBTZ)等金屬錯合物；2-(4-聯苯基)-5-(4-三級丁基苯基)-1，3，4-

二唑(簡稱：PBD)、1，3-雙[5-(對三級丁基苯基)-1，3，4-

二唑-2-基]苯(簡稱：OXD-7)、3-(4-聯苯基)-4-苯基-5-(4-三級丁基苯基)-1，2，4-三唑(簡稱：TAZ)、2，2’，2”-(1，3，5-苯三基)三(1-苯基-1H-苯并咪唑)(簡稱：TPBI)、紅啡啉(簡稱： BPhen)、浴銅靈(簡稱：BCP)、9-[4-(5-苯基-1，3，4-

二唑-2-基)苯基]-9H-咔唑(簡稱：CO11)等雜環化合物；4，4’-雙[N-(1-萘基)-N-苯基胺基]聯苯(簡稱：NPB或α-NPD)、N，N’-雙(3-甲基苯基)-N，N’-二苯基-[1，1’-聯苯]-4，4’-二胺(簡稱：TPD)、4，4’-雙[N-(螺-9，9’-聯茀-2-基)-N-苯基胺基]聯苯(簡稱：BSPB)等芳香胺化合物。另外，可以舉出蒽衍生物、菲衍生物、芘衍生物、

衍生物、二苯并[g，p]

衍生物等稠合多環芳香化合物(condensed polycyclic aromatic compound)。明確地說，可以舉出9，10-二苯基蒽(簡稱：DPAnth)、N，N-二苯基-9-[4-(10-苯基-9-蒽基)苯基]-9H-咔唑-3-胺(簡稱：CzA1PA)、4-(10-苯基-9-蒽基)三苯胺(簡稱：DPhPA)、4-(9H-咔唑-9-基)-4’-(10-苯基-9-蒽基)三苯胺(簡稱：YGAPA)、N，9-二苯基-N-[4-(10-苯基-9-蒽基)苯基]-9H-咔唑-3-胺(簡稱：PCAPA)、N，9-二苯基-N-{4-[4-(10-苯基-9-蒽基)苯基]苯基}-9H-咔唑-3-胺(簡稱：PCAPBA)、N，9-二苯基-N-(9，10-二苯基-2-蒽基)-9H-咔唑-3-胺(簡稱：2PCAPA)、6，12-二甲氧基-5，11-二苯

、N，N，N’，N’，N’’，N’’，N'''，N'''-八苯基二苯并[g，p]

-2，7，10，15-四胺(簡稱：DBC1)、9-[4-(10-苯基-9-蒽基)苯基]-9H-咔唑(簡稱：CzPA)、3，6-二苯基-9-[4-(10-苯基-9-蒽基)苯基]-9H-咔唑(簡稱：DPCzPA)、9，10-雙(3，5-二苯基苯基)蒽(簡稱：DPPA)、9，10-二(2-萘基)蒽(簡稱：DNA)、2-三級丁基-9，10-二(2-萘基)蒽(簡稱：t-BuDNA)、9，9’-聯蒽(簡稱：BANT)、9，9’-(二苯乙烯-3，3’-二基)二菲(簡稱：DPNS)、9，9’-(二苯乙烯-4，4’-二基)二菲(簡稱：DPNS2)以及1,3,5-三(1-芘基)苯(簡稱：TPB3)等。從這些物質及已知的物質中選擇一種或多種具有比上述化合物131及化合物132的能隙大的能隙的物質即可。 Although there is no particular limitation on the material (compound 135) that can be used for the light-emitting layer 130, for example, tris(8-hydroxyquinoline)aluminum(III) (abbreviated as: Alq), tris(4-methyl-8-hydroxyquinoline)aluminum(III) (abbreviated as: Almq ₃ ), bis(10-hydroxybenzo[h]quinoline)borate(II) (abbreviated as: BeBq ₂ ), bis(2-methyl-8-hydroxyquinoline)(4-phenylphenol)aluminum(III) (abbreviated as: BAlq), bis(8-hydroxyquinoline)zinc(II) (abbreviated as: Znq), bis[2-(2-benzo[h]quinoline)borate(II) (abbreviated as: BeBq 2 ),

Metal complexes such as bis[2-(2-benzothiazolyl)phenol]zinc(II) (abbreviated as ZnPBO), bis[2-(2-benzothiazolyl)phenol]zinc(II) (abbreviated as ZnBTZ); 2-(4-biphenyl)-5-(4-tert-butylphenyl)-1,3,4-

PBD), 1,3-bis[5-(p-tert-butylphenyl)-1,3,4-

oxadiazole-2-yl]benzene (abbreviation: OXD-7), 3-(4-biphenyl)-4-phenyl-5-(4-tert-butylphenyl)-1,2,4-triazole (abbreviation: TAZ), 2,2',2"-(1,3,5-benzenetriyl)tris(1-phenyl-1H-benzimidazole) (abbreviation: TPBI), red phenanthroline (abbreviation: BPhen), bathocophine (abbreviation: BCP), 9-[4-(5-phenyl-1,3,4-

Heterocyclic compounds such as oxadiazole-2-yl)phenyl]-9H-carbazole (abbreviated as CO11); aromatic amine compounds such as 4,4'-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (abbreviated as NPB or α-NPD), N,N'-bis(3-methylphenyl)-N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine (abbreviated as TPD), 4,4'-bis[N-(spiro-9,9'-bifluoren-2-yl)-N-phenylamino]biphenyl (abbreviated as BSPB). In addition, anthracene derivatives, phenanthrene derivatives, pyrene derivatives,

Derivatives, dibenzo[g,p]

Condensed polycyclic aromatic compounds such as derivatives. Specifically, 9,10-diphenylanthracene (DPAnth), N,N-diphenyl-9-[4-(10-phenyl-9-anthracenyl)phenyl]-9H-carbazole-3-amine (CzA1PA), 4-(10-phenyl-9-anthracenyl)triphenylamine (DPhPA), 4-(9H-carbazole-9-yl)-4'-(10-phenyl-9-anthracenyl)triphenylamine (YGAPA), N,9-diphenyl-N -[4-(10-phenyl-9-anthracenyl)phenyl]-9H-carbazole-3-amine (abbreviated as: PCAPA), N,9-diphenyl-N-{4-[4-(10-phenyl-9-anthracenyl)phenyl]phenyl}-9H-carbazole-3-amine (abbreviated as: PCAPBA), N,9-diphenyl-N-(9,10-diphenyl-2-anthracenyl)-9H-carbazole-3-amine (abbreviated as: 2PCAPA), 6,12-dimethoxy-5,11-diphenyl

、N，N，N'，N'，N''，N''，N'''，N'''-octaphenyldibenzo[g，p]

-2,7,10,15-tetramine (abbreviated as: DBC1), 9-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazole (abbreviated as: CzPA), 3,6-diphenyl-9-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazole (abbreviated as: DPCzPA), 9,10-bis(3,5-diphenylphenyl)anthracene (abbreviated as: DPPA), 9,10-di(2-naphthyl)anthracene ( The present invention relates to a novel molecule of the present invention, wherein the molecule is a ...

〈〈A pair of electrodes〉〉

The electrode 101 and the electrode 102 have the function of injecting holes and electrons into the light-emitting layer 130. The electrode 101 and the electrode 102 can be formed using metals, alloys, conductive compounds, and mixtures or stacks thereof. A typical example of a metal is aluminum (Al). In addition, transition metals such as silver (Ag), tungsten, chromium, molybdenum, copper, and titanium; alkali metals such as lithium (Li) or cesium; and Group 2 metals such as calcium or magnesium (Mg) can be used. As a transition metal, a rare earth metal such as ytterbium (Yb) can also be used. As an alloy, an alloy including the above-mentioned metals can be used, for example, MgAg, AlLi, etc. can be mentioned. As the conductive compound, for example, metal oxides such as indium tin oxide (hereinafter referred to as ITO), indium tin oxide containing silicon or silicon oxide (abbreviated as: ITSO), indium zinc oxide (Indium Zinc Oxide), and indium oxide containing tungsten and zinc can be cited. Inorganic carbon materials such as graphene can also be used as the conductive compound. As described above, one or both of the electrode 101 and the electrode 102 can be formed by stacking a plurality of these materials.

In addition, the light obtained from the light-emitting layer 130 is extracted through one or both of the electrode 101 and the electrode 102. Therefore, at least one of the electrode 101 and the electrode 102 has the function of transmitting visible light. As a conductive material having a light-transmitting function, a conductive material having a visible light transmittance of 40% or more and 100% or less, preferably 60% or more and 100% or less, and a resistivity of 1× ^10-2 Ω. cm or less can be cited. In addition, the electrode on the light-extracting side can also be formed of a conductive material having a light-transmitting function and a light-reflecting function. As the conductive material, a conductive material having a visible light reflectance of 20% or more and 80% or less, preferably 40% or more and 70% or less, and a resistivity of 1× ^10-2 Ω. cm or less can be cited. When a material with low light transmittance such as metal or alloy is used for the light extracting electrode, one or both of the electrode 101 and the electrode 102 may be formed with a thickness that allows visible light to pass therethrough (for example, a thickness of 1 nm to 10 nm).

Note that in this specification, etc., as an electrode having a light-transmitting function, a material having a function of transmitting visible light and having conductivity may be used, such as an oxide conductive layer represented by the above-mentioned ITO (Indium Tin Oxide), an oxide semiconductor layer, or an organic conductive layer containing organic substances. As an organic conductive layer containing organic substances, for example, a layer containing a composite material formed by mixing an organic compound and an electron donor (donor), a layer containing a composite material formed by mixing an organic compound and an electron acceptor (acceptor), etc. can be cited. In addition, the resistivity of the transparent conductive layer is preferably 1×10 ⁵ Ω. cm or less, and more preferably 1×10 ⁴ Ω. cm or less.

In addition, as a film forming method for the electrode 101 and the electrode 102, a sputtering method, an evaporation method, a printing method, a coating method, an MBE (Molecular Beam Epitaxy) method, a CVD method, a pulsed laser deposition method, an ALD (Atomic Layer Deposition) method, or the like can be applied.

〈〈Hole injection layer〉〉

The hole injection layer 111 has the function of reducing the injection barrier of holes from one of a pair of electrodes (electrode 101 or electrode 102) to promote hole injection, and is formed using, for example, a transition metal oxide, a phthalocyanine derivative, or an aromatic amine. Examples of the transition metal oxide include molybdenum oxide, vanadium oxide, ruthenium oxide, tungsten oxide, and manganese oxide. Examples of the phthalocyanine derivative include phthalocyanine or metal phthalocyanine. Examples of the aromatic amine include benzidine derivatives or phenylenediamine derivatives. Polymer compounds such as polythiophene or polyaniline may also be used, typically: poly(ethylenedioxythiophene)/poly(styrenesulfonic acid) as a self-doped polythiophene.

As the hole injection layer 111, a layer of a composite material composed of a hole transport material and a material having the property of receiving electrons from the hole transport material can be used. Alternatively, a stack of a layer containing a material having the property of receiving electrons and a layer containing a hole transport material can be used. In a steady state or in the presence of an electric field, charge transfer can be performed between these materials. As materials having the property of receiving electrons, organic acceptors such as quinone dimethane derivatives, tetrachlorobenzoquinone derivatives, and hexaazatriphenylbenzene derivatives can be cited. Specifically, compounds having an electron-withdrawing group (especially a halogen group such as a fluorine group, or a cyano group) such as 7,7,8,8-tetracyano-2,3,5,6-tetrafluoroquinodimethane (abbreviated as F ₄ -TCNQ), chloranil, 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazatriphenylene (abbreviated as HAT-CN), and 1,3,4,5,7,8-hexafluorotetracyano-naphthoquinodimethane (abbreviated as F6-TCNNQ) can be cited. In particular, compounds such as HAT-CN in which an electron-withdrawing group is bonded to a condensed aromatic ring having a plurality of heteroatoms are thermally stable and therefore are preferred. In addition, [3] ylidene derivatives containing electron-withdrawing groups (especially halogen groups such as fluorine groups and cyano groups) are particularly preferred because of their very high electron accepting properties. Specifically, α, α', α''-1,2,3-cycloalkanetriylidene tris[4-cyano-2,3,5,6-tetrafluorophenylacetonitrile], α, α', α''-1,2,3-cyclopropanetriylidene tris[2,6-dichloro-3,5-difluoro-4-(trifluoromethyl)phenylacetonitrile], α, α', α''-1,2,3-cycloalkanetriylidene tris[2,3,4,5,6-pentafluorophenylacetonitrile], etc. can be cited. In addition, transition metal oxides, such as oxides of Group 4 to Group 8 metals, can be used. Specifically, vanadium oxide, niobium oxide, tantalum oxide, chromium oxide, molybdenum oxide, tungsten oxide, manganese oxide, cerium oxide, etc. can be used. In particular, molybdenum oxide is preferably used because it is stable even in the atmosphere, has low hygroscopicity, and is easy to handle.

As the hole transport material, a material having a hole transport property higher than an electron transport property can be used, and preferably a material having a hole mobility of 1×10 ^-6 cm ² /Vs or more can be used. Specifically, aromatic amines and carbazole derivatives listed as hole transport materials that can be used for the light-emitting layer 130 can be used. In addition, aromatic hydrocarbons and stilbene derivatives can also be used. The above-mentioned hole transport material can also be a polymer compound.

Examples of the aromatic hydrocarbon include 2-tert-butyl-9,10-di(2-naphthyl)anthracene (abbreviation: t-BuDNA), 2-tert-butyl-9,10-di(1-naphthyl)anthracene, 9,10-bis(3,5-diphenylphenyl)anthracene (abbreviation: DPPA), 2-tert-butyl-9,10-bis(4-phenylphenyl)anthracene (abbreviation: t-BuDBA), 9,10-di(2-naphthyl)anthracene (abbreviation: DNA), 9,10-diphenylanthracene (abbreviation: DPAnth), 2-tert-butylanthracene (abbreviation: t-BuAnth), and 9,10-bis(4-methyl-1-naphthyl)anthracene (abbreviation: DMNA). , 2-tert-butyl-9,10-bis[2-(1-naphthyl)phenyl]anthracene, 9,10-bis[2-(1-naphthyl)phenyl]anthracene, 2,3,6,7-tetramethyl-9,10-di(1-naphthyl)anthracene, 2,3,6,7-tetramethyl-9,10-di(2-naphthyl)anthracene, 9,9'-bianthracene, 10,10'-diphenyl-9,9'-bianthracene, 10,10'-bis(2-phenylphenyl)-9,9'-bianthracene, 10,10'-bis[(2,3,4,5,6-pentaphenyl)phenyl]-9,9'-bianthracene, anthracene, fused tetraphenyl, rubrene, perylene, 2,5,8,11-tetra(tert-butyl)perylene, etc. In addition, fused pentadiene, coronene, etc. can also be used. Thus, it is more preferable to use an aromatic hydrocarbon having a hole mobility of 1×10 ^-6 cm ² /Vs or more and having 14 to 42 carbon atoms.

Note that the aromatic hydrocarbon may also have a vinyl skeleton. Examples of aromatic hydrocarbons having a vinyl group include 4,4'-bis(2,2-diphenylvinyl)biphenyl (abbreviation: DPVBi) and 9,10-bis[4-(2,2-diphenylvinyl)phenyl]anthracene (abbreviation: DPVPA).

In addition, polymer compounds such as poly(N-vinylcarbazole) (abbreviation: PVK), poly(4-vinyltriphenylamine) (abbreviation: PVTPA), poly[N-(4-{N’-[4-(4-diphenylamino)phenyl]phenyl-N’-phenylamino}phenyl)methacrylamide] (abbreviation: PTPDMA), and poly[N,N’-bis(4-butylphenyl)-N,N’-bis(phenyl)benzidine] (abbreviation: Poly-TPD) can also be used.

〈〈Hole Transport Layer〉〉

The hole transport layer 112 is a layer containing a hole transport material, and the materials exemplified as the materials of the hole injection layer 111 can be used. The hole transport layer 112 has a function of transporting holes injected into the hole injection layer 111 to the light emitting layer 130, and therefore preferably has a HOMO energy level that is the same as or close to that of the hole injection layer 111.

As the hole-transporting material, the materials exemplified as the materials of the hole injection layer 111 can be used. In addition, it is preferable to use a substance having a hole mobility of 1×10 ^-6 cm ² /Vs or more. However, as long as the hole-transporting property is higher than the electron-transporting property, a substance other than the above-mentioned substances can be used. In addition, the layer including the substance having high hole-transporting property is not limited to a single layer, and two or more layers composed of the above-mentioned substances can be stacked.

〈〈Electronic Transmission Layer〉〉

唑配體或噻唑配體的金屬錯合物。另外，可以舉出

二唑衍生物、三唑衍生物、啡啉衍生物、吡啶衍生物、聯吡啶衍生物、嘧啶衍生物等。另外，較佳為具有1×10^-6cm²/Vs以上的電子移動率的物質。但是，作為電子傳輸層，只要是電子傳輸性高於電洞傳輸性的物質，就可以採用上述以外的物質。另外，電子傳輸層118不限於單層，還可以層疊兩層以上的由上述物質構成的層。 The electron transport layer 118 has a function of transporting electrons injected from the other of the pair of electrodes (electrode 101 or electrode 102) through the electron injection layer 119 to the light-emitting layer 130. As the electron transport material, a material having higher electron transport than hole transport can be used, and preferably a material having an electron mobility of 1×10 ^-6 cm ² /Vs or more can be used. As a compound that easily receives electrons (a material having electron transport), a π-electron-deficient heteroaromatic compound such as a nitrogen-containing heteroaromatic compound or a metal complex can be used. Specifically, quinoline ligands, benzoquinoline ligands,

Azole ligands or thiazole ligands metal complexes. In addition,

Oxadiazole derivatives, triazole derivatives, phenanthroline derivatives, pyridine derivatives, bipyridine derivatives, pyrimidine derivatives, etc. In addition, it is preferably a substance having an electron mobility of 1×10 ^-6 cm ² /Vs or more. However, as the electron transport layer, as long as the electron transport property is higher than the hole transport property, a substance other than the above can be used. In addition, the electron transport layer 118 is not limited to a single layer, and two or more layers composed of the above substances can be stacked.

In addition, a layer for controlling the movement of electron carriers may be provided between the electron transport layer 118 and the light emitting layer 130. The layer for controlling the movement of electron carriers is a layer in which a small amount of a substance with high electron capture property is added to the above-mentioned material with high electron transport property, and the balance of carriers can be adjusted by suppressing the movement of electron carriers. This structure has a great effect on suppressing problems caused by electrons passing through the light emitting layer (such as a reduction in the life of the device).

〈〈Electron injection layer〉〉

The electron injection layer 119 has the function of lowering the injection barrier of electrons from the electrode 102 to promote electron injection, and for example, a Group 1 metal, a Group 2 metal, or their oxides, halides, carbonates, etc. can be used. A composite material of the above-mentioned electron conductive material and a material having the property of supplying electrons to the electron conductive material can also be used. As the material having the electron supply property, Group 1 metals, Group 2 metals, or their oxides, etc. can be cited. Specifically, alkaline metals, alkaline earth metals, or compounds of these metals such as lithium fluoride (LiF), sodium fluoride (NaF), cesium fluoride (CsF), calcium fluoride ( _CaF2 ), and lithium oxide ( _LiOx ) can be used. In addition, rare earth metal compounds such as erbium fluoride ( _ErF3 ) can be used. Alternatively, an electron salt may be used for the electron injection layer 119. Examples of the electron salt include a mixed oxide of calcium and aluminum to which electrons are added at a high concentration. Alternatively, a substance that can be used for the electron transport layer 118 may be used for the electron injection layer 119.

In addition, a composite material formed by mixing an organic compound with an electron donor can also be used for the electron injection layer 119. This composite material has excellent electron injection and electron transport properties because the electron donor generates electrons in the organic compound. In this case, the organic compound is preferably a material that has excellent performance in transporting the generated electrons. Specifically, for example, the substances constituting the electron transport layer 118 as described above (metal complexes, heteroaromatic compounds, etc.) can be used. As an electron donor, any substance that can donate electrons to the organic compound can be used. Specifically, it is preferred to use alkali metals, alkali earth metals, and rare earth metals, and lithium, cesium, magnesium, calcium, beryl, and yttrium can be mentioned. In addition, it is preferred to use an alkali metal oxide or an alkali earth metal oxide, and lithium oxide, calcium oxide, barium oxide, etc. can be mentioned. In addition, a Lewis base such as magnesium oxide can also be used. In addition, an organic compound such as tetrathiafulvalene (abbreviated as: TTF) can also be used.

In addition, the above-mentioned light-emitting layer, hole injection layer, hole transport layer, electron transport layer and electron injection layer can be formed by evaporation (including vacuum evaporation), inkjet method, coating method, nozzle printing method, gravure printing, etc. In addition, as the above-mentioned light-emitting layer, hole injection layer, hole transport layer, electron transport layer and electron injection layer, in addition to the above-mentioned materials, inorganic compounds such as quantum dots or high molecular compounds (oligomers, dendrimers, polymers, etc.) can also be used.

As quantum dots, colloidal quantum dots, alloy quantum dots, core-shell quantum dots, core-type quantum dots, etc. can be used. In addition, quantum dots containing element groups of Group 2 and Group 16, Group 13 and Group 15, Group 13 and Group 17, Group 11 and Group 17, or Group 14 and Group 15 can also be used. Alternatively, quantum dots containing elements such as cadmium (Cd), selenium (Se), zinc (Zn), sulfur (S), phosphorus (P), indium (In), tellurium (Te), lead (Pb), gallium (Ga), arsenic (As), aluminum (Al) can be used.

As the liquid medium used for wet treatment, for example, ketones such as methyl ethyl ketone and cyclohexanone; glycerol fatty acid esters such as ethyl acetate; halogenated aromatic hydrocarbons such as dichlorobenzene; aromatic hydrocarbons such as toluene, xylene, mesitylene, cyclohexylbenzene; fatty hydrocarbons such as cyclohexane, decahydronaphthalene, dodecane; and organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO).

Examples of polymer compounds that can be used in the light-emitting layer include polyphenylene vinylene (PPV) derivatives such as poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene vinylene] (abbreviated as MEH-PPV) and poly(2,5-dioctyl-1,4-phenylene vinylene); polyfluorene derivatives such as poly(9,9-di-n-octylfluorenyl-2,7-diyl) (abbreviated as PF8), poly[(9,9-di-n-octylfluorenyl-2,7-diyl)-alt-(benzo[2,1,3]thiadiazole-4,8-diyl)] (abbreviated as F8BT), poly[(9 , 9-dioctylfluorenyl-2,7-diyl)-alt-(2,2'-bithiophene-5,5'-diyl)] (abbreviated as F8T2), poly[(9,9-dioctyl-2,7-divinylfluorenylene)-alt-(9,10-anthracene)], poly[(9,9-dihexylfluorenyl-2,7-diyl)-alt-(2,5-dimethyl-1,4-phenylene)], etc.; polyalkylthiophene (PAT) derivatives such as poly(3-hexylthiophene-2,5-diyl) (abbreviated as P3HT), etc., polyphenylene derivatives, etc. In addition, the above-mentioned polymer compounds, PVK, poly(2-vinylnaphthalene), poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (abbreviated as: PTAA) and other polymer compounds may be doped with a luminescent compound and used in the luminescent layer. As the luminescent compound, the luminescent compounds exemplified above may be used.

〈〈Substrate〉〉

In addition, the light emitting element of one embodiment of the present invention can be manufactured on a substrate made of glass, plastic, etc. As the order of stacking on the substrate, the layers can be stacked sequentially from the electrode 101 side or from the electrode 102 side.

In addition, as a substrate for a light-emitting element that can form an embodiment of the present invention, for example, glass, quartz or plastic can be used. Alternatively, a flexible substrate can also be used. A flexible substrate is a substrate that can be bent, such as a plastic substrate made of polycarbonate or polyarylate. In addition, a thin film, an inorganic evaporated film, etc. can be used. Note that other materials can be used as long as they serve as a support in the manufacturing process of the light-emitting element and the optical element (color filter, etc.). Alternatively, any material can be used as long as it has the function of protecting the light-emitting element and the optical element.

For example, in this specification, etc., various substrates can be used to form a light-emitting element. There is no particular limitation on the type of substrate. As examples of the substrate, for example, a semiconductor substrate (for example, a single crystal substrate or a silicon substrate), an SOI substrate, a glass substrate, a quartz substrate, a plastic substrate, a metal substrate, a stainless steel substrate, a substrate with a stainless steel foil, a tungsten substrate, a substrate with a tungsten foil, a flexible substrate, a bonding film, a cellulose nanofiber (CNF) containing a fibrous material, paper or a base film, etc. can be used. As examples of glass substrates, there are barium borosilicate glass, aluminum borosilicate glass, sodium calcium glass, etc. As flexible substrates, bonding films, base films, etc., the following examples can be cited. For example, plastics represented by polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polyether sulfone (PES), and polytetrafluoroethylene (PTFE) can be cited. Alternatively, resins such as acrylic resins can be cited as an example. Alternatively, polypropylene, polyester, polyvinyl fluoride, or polyvinyl chloride can be cited as an example. Alternatively, polyamide, polyimide, aromatic polyamide, epoxy resin, inorganic vapor-deposited film, paper, etc. can be cited as an example.

In addition, a flexible substrate may be used as a substrate, and a light-emitting element may be directly formed on the flexible substrate. Alternatively, a peeling layer may be provided between the substrate and the light-emitting element. The peeling layer may be used when a part or all of the light-emitting element is manufactured on the peeling layer, and then it is separated from the substrate and transferred to another substrate. In this case, the light-emitting element may be transferred to a substrate or a flexible substrate having low heat resistance. In addition, as the above-mentioned peeling layer, for example, a stacked structure of an inorganic film of a tungsten film and a silicon oxide film or a structure in which a resin film such as polyimide is formed on a substrate may be used.

That is, a light-emitting element may be formed using one substrate and then transferred to another substrate. Examples of substrates to which the light-emitting element is transferred include, in addition to the above-mentioned substrates, cellophane substrates, stone substrates, wood substrates, cloth substrates (including natural fibers (silk, cotton, linen), synthetic fibers (nylon, polyurethane, polyester) or recycled fibers (acetate, cuprammonium, rayon, recycled polyester), etc.), leather substrates, rubber substrates, etc. By using these substrates, it is possible to manufacture light-emitting elements that are not easily damaged, light-emitting elements with high heat resistance, light-emitting elements that are lightweight, or light-emitting elements that are thin.

Alternatively, a field effect transistor (FET) may be formed on the substrate, and the light emitting element 150 may be manufactured on an electrode electrically connected to the FET. Thus, an active matrix display device in which the driving of the light emitting element is controlled by the FET may be manufactured.

The structure shown in this embodiment can be used in combination with the structures shown in other embodiments as appropriate.

Implementation Method 2

In this embodiment, an example of a method for synthesizing an organic compound applicable to a light-emitting device according to an embodiment of the present invention is described by taking organic compounds represented by general formulae (G1) and (G2) as examples.

<Method for synthesizing the organic compound represented by the general formula (G1)>

The organic compound represented by the general formula (G1) can be synthesized by a synthesis method utilizing various reactions. For example, it can be synthesized by the following synthesis schemes (S-1) and (S-2). By coupling compound 1, arylamine (compound 2) and arylamine (compound 3), a diamine compound (compound 4) is obtained.

Then, by coupling the diamine compound (Compound 4), the halogenated aryl group (Compound 5), and the halogenated aryl group (Compound 6), the organic compound represented by the above general formula (G1) can be obtained.

、菲、二苯乙烯、吖啶酮、啡

、啡噻

等。尤其較佳的是蒽、芘、香豆素、喹吖啶酮、苝、稠四苯、萘并雙苯并呋喃。 Note that in the above-mentioned synthesis schemes (S-1) and (S-2), A represents a substituted or unsubstituted fused aromatic ring having 10 to 30 carbon atoms or a substituted or unsubstituted fused heteroaromatic ring having 10 to 30 carbon atoms, ^Ar1 to ^Ar4 each independently represent a substituted or unsubstituted aromatic hydrocarbon group having 6 to 13 carbon atoms, and ^X1 to ^X8 each independently represent any one of an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms. Examples of the fused aromatic ring or fused heteroaromatic ring include:

, phenanthrene, stilbene, acridone, coffee

Morphothiocyanate

etc. Particularly preferred are anthracene, pyrene, coumarin, quinacridone, perylene, tetraphenylene, and naphthodibenzofuran.

Note that in the above-mentioned synthesis schemes (S-1) and (S-2), when the Buchwald-Hartwig reaction using a palladium catalyst is performed, ^X10 to ^X13 represent a halogen group or a trifluoromethanesulfonate group, and the halogen is preferably iodine, bromine or chlorine. In the above-mentioned reaction, palladium compounds such as bis(dibenzylideneacetone)palladium(0) and palladium(II) acetate, tri(tert-butyl)phosphine, tri(n-hexyl)phosphine, tricyclohexylphosphine, di(1-adamantane)-n-butylphosphine, and 2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl can be used as ligands. In addition, in the above reaction, organic bases such as sodium tertiary butoxide, inorganic bases such as potassium carbonate, cesium carbonate, sodium carbonate, etc. can be used. As a solvent, toluene, xylene, mesitylene, benzene, tetrahydrofuran, dioxane, etc. can be used. Note that the reagents that can be used in the above reaction are not limited to the above reagents.

The reaction performed in the above-mentioned synthesis schemes (S-1) and (S-2) is not limited to the Buchwald-Hartwig reaction, and the Ueda-Kosugi-Stille coupling reaction using an organotin compound, the coupling reaction using a Grignard reagent, the Ullmann reaction using copper or a copper compound, etc. can also be utilized.

In the above synthesis scheme (S-1), when compound 2 and compound 3 have different structures, it is preferred to react compound 1 with compound 2 to form a coupled product, and then react the obtained coupled product with compound 3. Note that, when compound 1 is reacted with compound 2 and compound 3 one by one, compound 1 is preferably a dihalide, and ^X10 and ^X11 are preferably subjected to amination reaction selectively one by one using different halogens.

Furthermore, in the above synthesis scheme (S-2), when compound 5 and compound 6 have different structures, it is preferred to react compound 4 with compound 5 to form a coupled product, and then react the obtained coupled product with compound 6.

Implementation method 3

In this embodiment, a light emitting element having a structure different from that of the light emitting element shown in Embodiment 1 is described with reference to FIG6. Note that in FIG6, the same shading is used for parts having the same functions as those of the element symbols shown in FIG1A, and the element symbols are sometimes omitted. In addition, parts having the same functions as those in FIG1A are represented by the same element symbols, and their detailed descriptions are sometimes omitted.

<Structural Example 2 of Light Emitting Element>

FIG. 6 is a schematic cross-sectional view of the light emitting element 250 .

The light-emitting element 250 shown in FIG6 has a plurality of light-emitting units (light-emitting unit 106 and light-emitting unit 108) between a pair of electrodes (electrode 101 and electrode 102). One of the plurality of light-emitting units preferably has the same structure as the EL layer 100 shown in FIG1A. That is, the light-emitting element 150 shown in FIG1A preferably has one light-emitting unit, and the light-emitting element 250 preferably has a plurality of light-emitting units. Note that in the light-emitting element 250, although the case where the electrode 101 is an anode and the electrode 102 is a cathode is described, the opposite structure may also be adopted as the structure of the light-emitting element 250.

In the light-emitting element 250 shown in FIG6 , the light-emitting unit 106 and the light-emitting unit 108 are stacked, and the charge generation layer 115 is provided between the light-emitting unit 106 and the light-emitting unit 108. In addition, the light-emitting unit 106 and the light-emitting unit 108 may have the same structure or different structures. For example, the light-emitting unit 108 preferably has the same structure as the EL layer 100.

The light emitting element 250 includes the light emitting layer 120 and the light emitting layer 170. The light emitting unit 106 includes a hole injection layer 111, a hole transport layer 112, an electron transport layer 113, and an electron injection layer 114 in addition to the light emitting layer 120. The light emitting unit 108 includes a hole injection layer 116, a hole transport layer 117, an electron transport layer 118, and an electron injection layer 119 in addition to the light emitting layer 170.

In the light-emitting element 250, any one of the light-emitting units 106 and 108 may contain the compound according to one embodiment of the present invention. Note that the light-emitting layer 120 or the light-emitting layer 170 is preferably the layer containing the compound.

The charge generation layer 115 may have a structure in which an acceptor substance serving as an electron acceptor is added to a hole transport material, or a structure in which a donor substance serving as an electron donor is added to an electron transport material. Alternatively, these two structures may be stacked.

When the charge generating layer 115 includes a composite material composed of an organic compound and an acceptor substance, the composite material that can be used for the hole injection layer 111 shown in Embodiment 1 may be used as the composite material. As the organic compound, various compounds such as aromatic amine compounds, carbazole compounds, aromatic hydrocarbons, and high molecular compounds (oligomers, dendrimers, polymers, etc.) may be used. In addition, as the organic compound, it is preferred to use a substance whose hole mobility is greater than 1×10 ^-6 cm ² /Vs. However, any substance other than these may be used as long as the hole transport property is higher than the electron transport property. Since the composite material composed of an organic compound and an acceptor substance has good carrier injection and carrier transport properties, low voltage drive and low current drive can be achieved. Note that when the surface of the anode side of the light-emitting unit contacts the charge generation layer 115, the charge generation layer 115 can also have the function of the hole injection layer or the hole transport layer of the light-emitting unit, so the hole injection layer or the hole transport layer may not be provided in the light-emitting unit. Alternatively, when the surface of the cathode side of the light-emitting unit contacts the charge generation layer 115, the charge generation layer 115 can also have the function of the electron injection layer or the electron transport layer of the light-emitting unit, so the electron injection layer or the electron transport layer may not be provided in the light-emitting unit.

Note that the charge generating layer 115 may also be a stacked structure of a layer of a composite material including an organic compound and an acceptor substance and a layer composed of other materials. For example, a layer of a composite material including an organic compound and an acceptor substance and a layer including a compound selected from electron-donating substances and a compound with high electron transport properties may be combined. Alternatively, a layer of a composite material including an organic compound and an acceptor substance and a layer including a transparent conductive film may be combined.

The charge generation layer 115 sandwiched between the light-emitting cell 106 and the light-emitting cell 108 only needs to have a structure that injects electrons into one light-emitting cell and injects holes into the other light-emitting cell when a voltage is applied between the electrode 101 and the electrode 102. For example, in FIG6 , when a voltage is applied in such a manner that the potential of the electrode 101 is higher than the potential of the electrode 102, the charge generation layer 115 injects electrons into the light-emitting cell 106 and injects holes into the light-emitting cell 108.

From the viewpoint of light extraction efficiency, the charge generation layer 115 preferably has visible light transmittance (specifically, the transmittance of visible light is 40% or more). In addition, the charge generation layer 115 functions even if its conductivity is lower than that of a pair of electrodes (electrode 101 and electrode 102).

By forming the charge generation layer 115 using the above-mentioned material, it is possible to suppress an increase in the driving voltage when light-emitting layers are stacked.

Although FIG6 illustrates a light-emitting element having two light-emitting units, the same structure can be applied to a light-emitting element having three or more light-emitting units stacked. As shown in the light-emitting element 250, by arranging a plurality of light-emitting units between a pair of electrodes in a manner separated by a charge generating layer, a light-emitting element can be realized that can emit light with high brightness while maintaining a low current density and has a longer life. In addition, a light-emitting element with low power consumption can also be realized.

In addition, in each of the above structures, the luminescent colors of the object materials used for the light-emitting unit 106 and the light-emitting unit 108 can be the same or different. When the light-emitting unit 106 and the light-emitting unit 108 include object materials having the function of emitting light of the same color, the light-emitting element 250 becomes a light-emitting element that exhibits high luminescence brightness at a lower current value, so it is preferred. In addition, when the light-emitting unit 106 and the light-emitting unit 108 include object materials having the function of emitting light of different colors from each other, the light-emitting element 250 emits light of multiple colors, so it is preferred. At this time, when multiple light-emitting materials with different luminescent wavelengths are used for one or both of the light-emitting layer 120 and the light-emitting layer 170, light with different luminescent peaks is synthesized, so the emission spectrum of the light-emitting element 250 has at least two maximum values.

The above structure is suitable for obtaining white luminescence. White luminescence can be obtained by making the light from the luminescent layer 120 and the light from the luminescent layer 170 complementary to each other. It is particularly preferred to select the object material in a manner that realizes white luminescence with high color rendering or luminescence with at least red, green, and blue.

It is preferred to use the structure of the light-emitting layer 130 shown in Embodiment 1 for one or both of the light-emitting layer 120 and the light-emitting layer 170. By adopting this structure, a light-emitting element with good light-emitting efficiency and reliability can be obtained. The guest material included in the light-emitting layer 130 is a fluorescent material and a phosphorescent material or a TADF material. Therefore, by using the structure of the light-emitting layer 130 shown in Embodiment 1 for one or both of the light-emitting layer 120 and the light-emitting layer 170, a light-emitting element with high efficiency, high reliability and multi-color light emission can be obtained.

In addition, in a light-emitting element in which more than three light-emitting units are stacked, the light-emitting color of the guest material used for each light-emitting unit can be the same or different. In the case where the light-emitting element includes multiple light-emitting units that emit light of the same color, these light-emitting units can obtain a light-emitting color with high light-emitting brightness at a lower current value than other colors. This structure is suitable for adjusting the light-emitting color. It is particularly preferred for use in the case of using guest materials with different light-emitting efficiencies and exhibiting different light-emitting colors. For example, in the case of setting three light-emitting units, by setting two light-emitting units including a fluorescent material exhibiting the same light-emitting color and one light-emitting unit including a phosphorescent material exhibiting a light-emitting color different from that of the fluorescent material, the light-emitting intensity of the fluorescent luminescence and the phosphorescent luminescence can be adjusted. In other words, the intensity of the luminous color can be adjusted according to the number of light-emitting units.

In the case of using the above-mentioned light-emitting element including two fluorescent light-emitting units and one phosphorescent light-emitting unit, in order to efficiently obtain white light, it is preferably to adopt the following structure: the light-emitting element includes two light-emitting units including blue fluorescent materials and one light-emitting unit including yellow phosphorescent materials; the light-emitting element includes two light-emitting units including blue fluorescent materials and one light-emitting unit including red phosphorescent materials and green phosphorescent materials; the light-emitting element includes two light-emitting units including blue fluorescent materials and one light-emitting unit including red phosphorescent materials, yellow phosphorescent materials and green phosphorescent materials. In this way, the light-emitting element and the phosphorescent light-emitting layer of an embodiment of the present invention can be appropriately combined.

In addition, at least one of the light-emitting layer 120 and the light-emitting layer 170 may be further divided into layers and each layer may contain a different light-emitting material. That is, at least one of the light-emitting layer 120 and the light-emitting layer 170 may be formed of two or more layers. For example, when the light-emitting layer is formed by stacking the first light-emitting layer and the second light-emitting layer in sequence from the hole transport layer side, a material having a hole transport property may be used as the main material of the first light-emitting layer, and a material having an electron transport property may be used as the main material of the second light-emitting layer. In this case, the light-emitting materials contained in the first light-emitting layer and the second light-emitting layer may be the same or different materials. In addition, the luminescent materials included in the first luminescent layer and the second luminescent layer may be materials having the function of emitting light of the same color or materials having the function of emitting light of different colors. By adopting a structure in which a plurality of luminescent materials having the function of emitting light of different colors are used, white light with high color rendering properties composed of three primary colors or four or more luminescent colors can be obtained.

This implementation method can be appropriately combined with other implementation methods.

Implementation Method 4

In this embodiment, a light emitting device using the light emitting element described in Embodiment 1 and Embodiment 3 will be described with reference to FIG. 7A and FIG. 7B .

FIG7A is a top view of the light emitting device, and FIG7B is a cross-sectional view cut along A-B and C-D in FIG7A. The light emitting device includes a driving circuit portion (source side driving circuit) 601 for controlling the light emission of the light emitting element, a pixel portion 602, and a driving circuit portion (gate side driving circuit) 603, which are indicated by dotted lines. In addition, component symbol 604 is a sealing substrate, component symbol 625 is a desiccant, component symbol 605 is a sealant, and the inner side surrounded by the sealant 605 is a space 607.

In addition, the guide wiring 608 is used to transmit the signal input to the source side driving circuit 601 and the gate side driving circuit 603, and receives the video signal, clock signal, start signal, reset signal, etc. from the FPC (flexible printed circuit) 609 used as an external input terminal. In addition, although only the FPC is shown here, the FPC can also be installed with a printed wiring board (PWB). The light-emitting device in this specification includes not only the light-emitting device body, but also the light-emitting device installed with the FPC or PWB.

Next, the cross-sectional structure of the light emitting device will be described with reference to Fig. 7B. A driver circuit section and a pixel section are formed on an element substrate 610, and a source-side driver circuit 601 as the driver circuit section and one pixel in the pixel section 602 are shown here.

In addition, in the source side driver circuit 601, a CMOS circuit combining an n-channel TFT 623 and a p-channel TFT 624 is formed. In addition, the driver circuit can also be formed using various CMOS circuits, PMOS circuits, or NMOS circuits. In addition, in the present embodiment, although a driver-integrated type in which the driver circuit is formed on the substrate is shown, this structure does not necessarily have to be adopted, and the driver circuit can also be formed outside instead of being formed on the substrate.

The pixel portion 602 is formed of a pixel including a switching TFT 611, a current control TFT 612, and a first electrode 613 electrically connected to the drain of the current control TFT 612. An insulator 614 is formed to cover an end of the first electrode 613. The insulator 614 can be formed using a positive photosensitive resin film.

In order to improve the coverage of the film formed on the insulator 614, the upper end or the lower end of the insulator 614 is formed into a curved surface having a curvature. For example, when a photosensitive acrylic resin is used as the material of the insulator 614, it is preferred that only the upper end of the insulator 614 has a curved surface. The radius of curvature of the curved surface is greater than or equal to 0.2 μm and less than or equal to 0.3 μm. In addition, as the insulator 614, a negative photosensitive material or a positive photosensitive material can be used.

An EL layer 616 and a second electrode 617 are formed on the first electrode 613. Here, as the material of the first electrode 613 serving as an anode, a material having a large work function is preferably used. For example, in addition to a single-layer film such as an ITO film, an indium tin oxide film containing silicon, an indium oxide film containing 2 wt% or more and 20 wt% or less of zinc oxide, a titanium nitride film, a chromium film, a tungsten film, a Zn film, and a Pt film, a stacked film composed of a titanium nitride film and a film containing aluminum as a main component, and a three-layer stacked film composed of a titanium nitride film, a film containing aluminum as a main component, and a titanium nitride film can also be used. Note that when a stacked structure is used, the wiring resistance is also low, good ohmic contact can be obtained, and it can be used as an anode.

The EL layer 616 is formed by various methods such as evaporation using an evaporation mask, inkjet, spin coating, etc. As a material constituting the EL layer 616, a low molecular compound or a high molecular compound (including an oligomer and a dendrimer) may be used.

In addition, as a material of the second electrode 617 formed on the EL layer 616 and used as a cathode, it is preferable to use a material with a small work function (Al, Mg, Li, Ca, or alloys and compounds thereof, MgAg, MgIn, AlLi, etc.). Note that when light generated in the EL layer 616 is allowed to pass through the second electrode 617, it is preferable to use a stacked layer composed of a metal thin film with a reduced film thickness and a transparent conductive film (ITO, indium oxide containing 2 wt% or more and 20 wt% or less of zinc oxide, indium tin oxide containing silicon, zinc oxide (ZnO), etc.) as the second electrode 617.

In addition, the light-emitting element 618 is formed by the first electrode 613, the EL layer 616, and the second electrode 617. The light-emitting element 618 preferably has the structure described in Embodiment 1 and Embodiment 3. In addition, the pixel portion includes a plurality of light-emitting elements, and the light-emitting device of this embodiment may include both the light-emitting elements having the structures described in Embodiment 1 and Embodiment 3 and the light-emitting elements having other structures.

Furthermore, by bonding the sealing substrate 604 and the element substrate 610 together using the sealant 605, a light-emitting element 618 is provided in a space 607 surrounded by the element substrate 610, the sealing substrate 604, and the sealant 605. In addition, the space 607 is filled with a filler, and in addition to being filled with an inert gas (nitrogen, argon, etc.), it is sometimes filled with a resin or a dry material, or both a resin and a dry material.

As the sealant 605, epoxy resin or glass powder is preferably used. In addition, these materials are preferably materials that do not allow moisture and oxygen to pass through as much as possible. In addition, as a material for the sealing substrate 604, in addition to a glass substrate and a quartz substrate, a plastic substrate composed of FRP (Fiber Reinforced Plastics: glass fiber reinforced plastic), PVF (polyvinyl fluoride), polyester or acrylic resin can also be used.

By the above method, a light-emitting device using the light-emitting element described in Embodiment 1 and Embodiment 3 can be obtained.

<Structural Example 1 of Light Emitting Device>

In FIG. 8A and FIG. 8B, as an example of a display device, an example of a light-emitting device in which a light-emitting element emitting white light and a color layer (color filter) are formed is shown.

8A shows a substrate 1001, a base insulating film 1002, a gate insulating film 1003, gate electrodes 1006, 1007, 1008, a first interlayer insulating film 1020, a second interlayer insulating film 1021, a peripheral portion 1042, a pixel portion 1040, a driving circuit portion 1041, a first electrode 1024W, 1024R, 1024G, 1024B of a light-emitting element, a partition wall 1025, an EL layer 1028, a second electrode 1029 of the light-emitting element, a sealing substrate 1031, a sealant 1032, and the like.

In addition, in FIG8A and FIG8B , color layers (red color layer 1034R, green color layer 1034G, blue color layer 1034B) are provided on a transparent substrate 1033. In addition, a black layer (black matrix) 1035 may be provided. The transparent substrate 1033 provided with the color layers and the black layer is aligned and fixed on the substrate 1001. In addition, the color layers and the black layer are covered by a cover layer 1036. 8A shows that light does not pass through the color layer but is transmitted to the external light-emitting layer and light passes through the color layers of each color and is transmitted to the external light-emitting layer. The light that does not pass through the color layer becomes white light and the light that passes through the color layer becomes red light, blue light, and green light, so that images can be displayed with pixels of four colors.

8B shows an example in which a red color layer 1034R, a green color layer 1034G, and a blue color layer 1034B are formed between the gate insulating film 1003 and the first interlayer insulating film 1020. As shown in FIG8B, the color layers may be provided between the substrate 1001 and the sealing substrate 1031.

In addition, although the light-emitting device described above is a light-emitting device having a structure in which light is emitted from the substrate 1001 side on which TFTs are formed (bottom emission type), a light-emitting device having a structure in which light is emitted from the sealing substrate 1031 side (top emission type) may also be used.

<Structural Example 2 of Light Emitting Device>

9A and 9B show cross-sectional views of a top-emitting light-emitting device. In this case, a substrate that does not allow light to pass through can be used as the substrate 1001. The process up to the manufacture of the connecting electrode connecting the TFT and the anode of the light-emitting element is carried out in the same manner as the bottom-emitting light-emitting device. Then, a third interlayer insulating film 1037 is formed in a manner covering the electrode 1022. The insulating film may also have a planarizing function. The third interlayer insulating film 1037 may be formed using the same material as the second interlayer insulating film 1021 or various other materials.

Although the lower electrode 1025W, the lower electrode 1025R, the lower electrode 1025G, and the lower electrode 1025B of the light-emitting element are all anodes here, they can also be cathodes. In addition, in the top emission type light-emitting device shown in Figures 9A and 9B, it is preferred that the lower electrode 1025W, the lower electrode 1025R, the lower electrode 1025G, and the lower electrode 1025B are reflective electrodes. In addition, it is preferred that the second electrode 1029 has the function of emitting light and allowing light to pass. In addition, it is preferred to use a microcavity structure between the second electrode 1029 and the lower electrodes 1025W, 1025R, 1025G, and 1025B to amplify light of a specific wavelength. The structure of the EL layer 1028 is the same as that described in Embodiment 1 and Embodiment 3, and an element structure capable of obtaining white light emission is used.

In Figs. 8A and 8B and Figs. 9A and 9B, a structure of an EL layer capable of obtaining white luminescence may be realized by using a plurality of luminescent layers or a plurality of luminescent units, etc. Note that the structure for obtaining white luminescence is not limited to this.

When the top emission structure shown in FIG. 9A and FIG. 9B is adopted, a sealing substrate 1031 provided with color layers (red color layer 1034R, green color layer 1034G, blue color layer 1034B) can be used for sealing. A black layer (black matrix) 1030 located between pixels can be provided on the sealing substrate 1031. The color layers (red color layer 1034R, green color layer 1034G, blue color layer 1034B) and the black layer (black matrix) can also be covered by a cover layer. In addition, a light-transmitting substrate is used as the sealing substrate 1031.

In addition, although FIG. 9A shows a structure for full-color display in three colors of red, green, and blue, as shown in FIG. 9B , full-color display may be performed in four colors of red, green, blue, and white. In addition, the structure for full-color display is not limited to these structures. For example, full-color display may be performed in four colors of red, green, blue, and yellow.

According to a light-emitting element of an embodiment of the present invention, a fluorescent material and a phosphorescent material or a TADF material are used as a guest material, thereby achieving high-efficiency multi-color luminescence. Therefore, by using the light-emitting element in the light-emitting device shown in this embodiment, a light-emitting device with high luminescence efficiency can be obtained.

By the above method, a light-emitting device using the light-emitting element described in Embodiment 1 and Embodiment 3 can be obtained.

In addition, this embodiment can be appropriately combined with other embodiments.

Implementation Method 5

In this embodiment, an electronic device and a display device according to an embodiment of the present invention are described.

According to one embodiment of the present invention, an electronic device and a display device having a flat surface, high luminous efficiency and high reliability can be manufactured. According to one embodiment of the present invention, an electronic device and a display device having a curved surface, high luminous efficiency and high reliability can be manufactured. In addition, as described above, a light-emitting element with high color reproducibility can be obtained.

Examples of electronic devices include televisions; desktop or laptop personal computers; displays for computers, etc.; digital cameras; digital video cameras; digital photo frames; mobile phones; portable game consoles; portable information terminals; audio playback devices; large game consoles such as pinball machines, etc.

The portable information terminal 900 shown in FIG. 10A and FIG. 10B includes a housing 901, a casing 902, a display portion 903, a hinge portion 905, and the like.

The housing 901 and the housing 902 are connected together by a hinge 905. The portable information terminal 900 can be transformed from a folded state (FIG. 10A) to an unfolded state as shown in FIG10B. Thus, the portable terminal 900 has good portability when carried, and has a large display area, so the visibility when in use is high.

The portable information terminal 900 is provided with a flexible display portion 903 across a housing 901 and a housing 902 connected by a hinge portion 905.

The light emitting device manufactured using one embodiment of the present invention can be used for the display portion 903. Thus, a highly reliable portable information terminal can be manufactured.

The display unit 903 can display at least one of document information, still images, and moving images, etc. When the document information is displayed on the display unit 903, the portable information terminal 900 can be used as an electronic book reader.

When the portable information terminal 900 is unfolded, the display portion 903 is maintained in a state where the radius of curvature is large. For example, the display portion 903 may be maintained in a manner including a portion that is bent with a radius of curvature of 1 mm or more and 50 mm or less, preferably 5 mm or more and 30 mm or less. A portion of the display portion 903 is continuously provided with pixels across the housing 901 and the housing 902, thereby enabling curved display.

The display portion 903 is used as a touch panel and can be operated with a finger, a touch pen, or the like.

The display unit 903 is preferably formed of a flexible display. Thus, continuous display can be performed across the housing 901 and the housing 902. In addition, the housing 901 and the housing 902 may be provided with displays respectively.

In order to prevent the angle formed by the housing 901 and the housing 902 from exceeding a predetermined angle when the portable information terminal 900 is unfolded, the hinge part 905 preferably has a locking mechanism. For example, the locking angle (at which the terminal cannot be opened further) is preferably greater than 90° and less than 180°, and typically can be 90°, 120°, 135°, 150°, or 175°, etc. Thus, the convenience, safety, and reliability of the portable information terminal 900 can be improved.

When the hinge portion 905 has the above-described locking mechanism, it is possible to suppress excessive force from being applied to the display portion 903, thereby preventing damage to the display portion 903. Thus, a highly reliable portable information terminal can be realized.

Housing 901 and housing 902 may also include a power button, an operation button, an external connection port, a speaker, a microphone, etc.

Either housing 901 or housing 902 may be provided with a wireless communication module, and data may be sent and received via a computer network such as the Internet, a local area network (LAN), or wireless fidelity (Wi-Fi: a registered trademark).

The portable information terminal 910 shown in FIG. 10C includes a housing 911, a display portion 912, operation buttons 913, an external connection port 914, a speaker 915, a microphone 916, a camera 917, and the like.

The light emitting device manufactured using one embodiment of the present invention can be used for the display portion 912. Thus, the portable information terminal can be manufactured with a high yield.

In the portable information terminal 910, a touch sensor is provided in the display portion 912. By touching the display portion 912 with a finger or a stylus pen, various operations such as making a call and inputting text can be performed.

In addition, by operating the operation button 913, the power can be turned on and off or the type of image displayed on the display portion 912 can be switched. For example, the e-mail writing screen can be switched to the main menu screen.

In addition, by providing a detection device such as a gyroscope sensor or an acceleration sensor inside the portable information terminal 910, the direction (vertical or horizontal) of the portable information terminal 910 can be determined, and the screen display direction of the display unit 912 can be automatically switched. In addition, the screen display direction can also be switched by touching the display unit 912, operating the operation button 913, or using the microphone 916 to input sound.

The portable information terminal 910 has one or more functions selected from a phone, a notebook, an information reading device, etc. Specifically, the portable information terminal 910 can be used as a smart phone. The portable information terminal 910 can execute various applications such as mobile phone, e-mail, article reading and editing, music playback, animation playback, Internet communication, computer games, etc.

10D includes a housing 921, a display portion 922, operation buttons 923, a shutter button 924, etc. In addition, the camera 920 is equipped with a detachable lens 926.

The light emitting device manufactured by one embodiment of the present invention can be used for the display portion 922. Thus, a camera with high reliability can be manufactured.

Here, although the camera 920 has a structure in which the lens 926 can be removed from the housing 921 and exchanged, the lens 926 and the housing 921 may be formed as one body.

The camera 920 can take still images or moving images by pressing the shutter button 924. In addition, the display unit 922 can also have a touch panel function, and the image can be taken by touching the display unit 922.

In addition, camera 920 can also have flash device and viewfinder etc. installed separately.In addition, these components can also be assembled in housing 921.

FIG. 11A is a schematic diagram showing an example of a sweeping robot.

The sweeping robot 5100 includes a display 5101 on the top and a plurality of cameras 5102, a brush 5103, and an operation button 5104 on the side. Although not shown, tires and a suction port are provided on the bottom of the sweeping robot 5100. In addition, the sweeping robot 5100 also includes various sensors such as an infrared sensor, an ultrasonic sensor, an acceleration sensor, a piezoelectric inductor, a photo sensor, and a gyroscope sensor. In addition, the sweeping robot 5100 includes a wireless communication unit.

The sweeping robot 5100 can walk automatically, detect garbage 5120, and suck the garbage from a suction port on the bottom.

In addition, the sweeping robot 5100 can determine the presence or absence of obstacles such as walls, furniture, or steps by analyzing the image taken by the camera 5102. In addition, when objects such as wiring that may be wrapped around the brush 5103 are detected through image analysis, the rotation of the brush 5103 can be stopped.

The remaining battery power and the amount of attracted garbage, etc. can be displayed on the display 5101. In addition, the walking path of the sweeping robot 5100 can also be displayed on the display 5101. In addition, the display 5101 can be a touch panel, and the operation button 5104 can be displayed on the display 5101.

The sweeping robot 5100 can communicate with a portable electronic device 5140 such as a smartphone. The image captured by the camera 5102 can be displayed on the portable electronic device 5140. Therefore, the owner of the sweeping robot 5100 can know the situation of the room when going out. In addition, the display content of the display 5101 can be confirmed using the portable electronic device 5140 such as a smartphone.

A light-emitting device according to an embodiment of the present invention can be used in a display 5101.

The robot 2100 shown in FIG. 11B includes a computing device 2110 , an illumination sensor 2101 , a microphone 2102 , an upper camera 2103 , a speaker 2104 , a display 2105 , a lower camera 2106 , an obstacle sensor 2107 , and a moving mechanism 2108 .

The microphone 2102 has a function of detecting the user's voice and surrounding sounds, etc. In addition, the speaker 2104 has a function of emitting sounds. The robot 2100 can communicate with the user using the microphone 2102 and the speaker 2104.

The display 2105 has the function of displaying various information. The robot 2100 can display the information desired by the user on the display 2105. The display 2105 can be equipped with a touch panel. The display 2105 can be a detachable information terminal. By setting the information terminal at a predetermined position of the robot 2100, charging and data transmission and reception can be performed.

The upper camera 2103 and the lower camera 2106 have the function of photographing the surrounding environment of the robot 2100. In addition, the obstacle sensor 2107 can detect the presence or absence of obstacles in front of the robot 2100 when the robot 2100 moves using the moving mechanism 2108. The robot 2100 can recognize the surrounding environment using the upper camera 2103, the lower camera 2106, and the obstacle sensor 2107 and move safely.

A light emitting device according to an embodiment of the present invention may be used in a display 2105 .

Fig. 11C is a diagram showing an example of a goggles-type display. The goggles-type display includes, for example, a housing 5000, a display portion 5001, a speaker 5003, an LED lamp 5004, an operation key 5005 (including a power switch or an operation switch), a connection terminal 5006, a sensor 5007 (which has a function of measuring the following factors: force, displacement, position, velocity, acceleration, angular velocity, rotation speed, distance, light, liquid, magnetism, temperature, chemical substance, sound, time, hardness, electric field, current, voltage, electricity, radiation, flow, humidity, inclination, vibration, smell or infrared), a microphone 5008, a second display portion 5002, a support portion 5012, an earphone 5013, and the like.

The light emitting device of one embodiment of the present invention can be used in the display portion 5001 and the second display portion 5002.

12A and 12B show a foldable portable information terminal 5150. The foldable portable information terminal 5150 includes a housing 5151, a display area 5152, and a bent portion 5153. FIG. 12A shows the portable information terminal 5150 in an unfolded state. FIG. 12B shows the portable information terminal 5150 in a folded state. Although the portable information terminal 5150 has a large display area 5152, by folding the portable information terminal 5150, the portable information terminal 5150 becomes smaller and more portable.

The display area 5152 can be folded into half by the curved portion 5153. The curved portion 5153 is composed of a retractable member and a plurality of supporting members. When folding, the retractable member is stretched so that the curved portion 5153 has a curvature radius of more than 2 mm, preferably more than 5 mm.

In addition, the display area 5152 may also be a touch panel (input/output device) equipped with a touch sensor (input device). The light emitting device of one embodiment of the present invention may be used for the display area 5152.

This implementation method can be appropriately combined with other implementation methods.

Implementation Method 6

In this embodiment, an example of applying a light emitting element according to an embodiment of the present invention to various lighting devices is described with reference to Fig. 13. By using the light emitting element according to an embodiment of the present invention, a lighting device with high light emitting efficiency and reliability can be manufactured.

By forming a light-emitting element according to an embodiment of the present invention on a flexible substrate, an electronic device or lighting equipment having a light-emitting area on a curved surface can be realized.

In addition, a light-emitting device to which a light-emitting element according to an embodiment of the present invention is applied can also be applied to automobile lighting, wherein the lighting is provided on a windshield, a ceiling, or the like.

FIG13 is an example of using a light-emitting element in an indoor lighting device 8501. In addition, since the light-emitting element can be large-sized, a large-area lighting device can also be formed. In addition, a lighting device 8502 having a curved surface in the light-emitting area can be formed by using a shell having a curved surface. The light-emitting element shown in this embodiment is in the form of a film, so the design of the shell is highly flexible. Therefore, a lighting device that can correspond to various designs can be formed. In addition, a large lighting device 8503 can also be installed on the indoor wall. Touch sensors can also be installed in the lighting device 8501, the lighting device 8502, and the lighting device 8503 to start or turn off the power.

In addition, by using the light emitting element on the surface side of the table, it is possible to provide a lighting device 8504 having the function of a table. In addition, by using the light emitting element on a part of other furniture, it is possible to provide a lighting device having the function of furniture.

As described above, by applying the light emitting device of one embodiment of the present invention, a lighting device and an electronic device can be obtained. Note that the present invention is not limited to the lighting device and the electronic device shown in this embodiment, but can be applied to lighting devices and electronic devices in various fields.

The structure shown in this embodiment can be used in combination with the structures shown in other embodiments as appropriate.

Embodiment 1

In this embodiment, a light-emitting element of an embodiment of the present invention and a comparative light-emitting element are described as well as the characteristics of the light-emitting element. The structure of the light-emitting element manufactured in this embodiment is the same as that of FIG. 1A. Tables 1 and 2 show the details of the element structure. The structures and abbreviations of the compounds used are shown below.

[Table 2]

〈Manufacturing of light-emitting devices〉

The following is a method for manufacturing the light-emitting element manufactured in this embodiment.

<<Manufacturing of Light-Emitting Element 1>>

An ITSO film having a thickness of 70 nm was formed on a glass substrate as the electrode 101. The electrode area of the electrode 101 was 4 mm ² (2 mm×2 mm).

Next, as the hole injection layer 111, DBT3P-II and molybdenum oxide (MoO ₃ ) were co-deposited on the electrode 101 at a weight ratio (DBT3P-II:MoO ₃ ) of 1:0.5 and a thickness of 40 nm.

Next, PCCP was evaporated on the hole injection layer 111 to a thickness of 20 nm as the hole transport layer 112.

Next, as the light-emitting layer 130, 4,6mCzP2Pm, Ir(ppz) ₃ , 2-trimethylsilyl-N,N,N',N'-tetrakis(3,5-di-tert-butylphenyl)-9,10-anthracenediamine (abbreviated as: 2TMS-mmtBuDPhA2Anth), and Ir(dmdppr-dmp) ₂ (dpm) were co-evaporated on the hole transport layer 112 in a weight ratio (4,6mCzP2Pm:Ir(ppz) ₃ :2TMS-mmtBuDPhA2Anth:Ir(dmdppr-dmp) ₂ (dpm)) of 0.8:0.2:0.025:0.01 and a thickness of 40 nm. In the light emitting layer 130, 4,6mCzP2Pm and Ir(ppz) ₃ are a combination that forms an excimer complex. In addition, 2TMS-mmtBuDPhA2Anth is a fluorescent material having a protective group, and Ir(dmdppr-dmp) ₂ (dpm) is a phosphorescent material containing Ir.

Next, 4,6mCzP2Pm was evaporated to a thickness of 20nm and NBPhen was evaporated to a thickness of 10nm on the light emitting layer 130 as the electron transport layer 118. Next, LiF was evaporated to a thickness of 1nm on the electron transport layer 118 as the electron injection layer 119.

Next, aluminum (Al) is formed to a thickness of 200 nm on the electron injection layer 119 as the electrode 102.

Next, in a glove box in a nitrogen atmosphere, a sealing glass substrate is fixed to the glass substrate on which the organic material is formed using a sealing agent for organic EL, thereby sealing the light-emitting element 1. Specifically, the sealing agent is applied around the organic material formed on the glass substrate, the glass substrate and the sealing glass substrate are bonded together, and ultraviolet light with a wavelength of 365 nm is irradiated at 6 J/ ^cm2 , and a heat treatment is performed at 80°C for 1 hour. The light-emitting element 1 is obtained by the above process.

<<Manufacturing of Light-Emitting Elements 2 to 4 and Comparative Light-Emitting Element 5>>

The only difference between light-emitting elements 2 to 4 and comparative light-emitting element 5 and the light-emitting element 1 is the structure of the light-emitting layer 130, and the other processes are the same as the manufacturing method of the light-emitting element 1. The details of the element structure are described in Tables 1 and 2, so the details of the manufacturing method are omitted. In light-emitting elements 1 to 4, the materials used in the light-emitting layer 130 are the same, but the mixing ratios thereof are different from each other. In addition, 2TMS-mmtBuDPhA2Anth, a fluorescent material having a protective group, is used in the comparative light-emitting element 5, but Ir(dmdppr-dmp) ₂ (dpm) as a phosphorescent material is not used.

〈Characteristics of light-emitting elements〉

Next, the characteristics of the light-emitting elements 1 to 4 and the comparative light-emitting element 5 manufactured as described above were measured. A colorimeter (BM-5A manufactured by Topcon Technohouse) was used for the measurement of brightness and CIE chromaticity. A multi-channel spectrometer (PMA-11 manufactured by Hamamatsu Photonics Co., Ltd.) was used for the measurement of electroluminescence spectrum.

FIG14 shows the external quantum efficiency-brightness characteristics of light-emitting elements 1 to 4 and comparative light-emitting element 5. FIG15 shows the electroluminescence spectrum when a current of 2.5 mA/ ^cm2 is passed through light-emitting elements 1 to 4 and comparative light-emitting element 5. The measurement of each light-emitting element was performed at room temperature (an atmosphere maintained at 23°C). FIG16 shows the absorption spectrum and emission spectrum of a toluene solution of 2TMS-mmtBuDPhA2Anth used for light-emitting elements 1 to 4, the absorption spectrum of a dichloromethane solution of Ir(dmdppr-dmp) ₂ (dpm), and the EL spectrum of comparative light-emitting element 9 described later (EL spectrum of an excited complex formed by 4,6mCzP2Pm and Ir(ppz) ₃ ).

The absorption spectrum of the toluene solution of 2TMS-mmtBuDPhA2Anth and the absorption spectrum of the dichloromethane solution of Ir(dmdppr-dmp) ₂ (dpm) were measured using an ultraviolet-visible spectrophotometer (V550 model manufactured by JASCO Corporation). The absorption spectrum shown in FIG16 is obtained by subtracting the absorption spectra of the toluene solution of 2TMS-mmtBuDPhA2Anth and the dichloromethane solution of Ir(dmdppr-dmp) _{2 (dpm) from the absorption spectra of the toluene solution of 2TMS-mmtBuDPhA2Anth and the dichloromethane solution of Ir(dmdppr-dmp) 2} (dpm) from the spectra measured by placing only the solvent in a quartz dish. The emission spectrum was measured using a fluorescent spectrophotometer (FS920 manufactured by Hamamatsu Photonics Co., Ltd.).

Table 3 shows the device characteristics of Light Emitting Elements 1 to 4 and Comparative Light Emitting Element 5 at around 1000 cd/m ² .

As shown in FIG. 15 , it can be seen that the emission spectra of light-emitting elements 1 to 4 have two peaks near 530 nm and near 610 nm. The peak near 530 nm originates from 2TMS-mmtBuDPhA2Anth, and the peak near 610 nm originates from Ir(dmdppr-dmp) ₂ (dpm). In other words, it can be seen that light-emitting elements 1 to 4 both emit light originating from 2TMS-mmtBuDPhA2Anth and emit light originating from Ir(dmdppr-dmp) ₂ (dpm). On the other hand, green light with a peak wavelength of 534 nm and a half-width of 65 nm is obtained in comparison light-emitting element 5. Therefore, it can be seen that light originating from 2TMS-mmtBuDPhA2Anth is obtained in comparison light-emitting element 5.

In addition, as shown in FIG. 14 , although light-emitting elements 1 to 4 and comparative light-emitting element 5 exhibit light emission from the fluorescent material, they have high light emission efficiency, that is, have an external quantum efficiency exceeding 20%. Here, the maximum generation probability of singlet excitons generated by the recombination of carriers (holes and electrons) injected from a pair of electrodes is 25%, so when the light extraction efficiency to the outside is 25%, the maximum external quantum efficiency of a conventional fluorescent light-emitting element is 6.25%. In addition, for example, the external quantum efficiency of an EL element when a fluorescent material and a phosphorescent material emit light at a ratio of 1:1 is 15.5%. However, compared with the case where only singlet excitons contribute to light emission or the case where both conventional fluorescent materials and phosphorescent materials contribute to light emission, light-emitting elements 1 to 4 and comparative light-emitting element 5 exhibit higher efficiency. This is because, in addition to the luminescence from singlet excitons generated by the recombination of carriers (holes and electrons) injected from a pair of electrodes, luminescence from energy transfer of triplet excitons or luminescence from singlet excitons generated from triplet excitons via antisystem crossing in an excited complex is also obtained. Therefore, it can be said that in a light-emitting element using a fluorescent material having a protective group, the non-radiative deactivation of triplet excitons is suppressed, and both singlet excitation energy and triplet excitation energy are efficiently converted into luminescence. That is, light-emitting elements 1 to 4 and comparative light-emitting element 5 can be regarded as light-emitting elements using ExEF.

In addition, as shown in FIG. 14 and FIG. 15, the light-emitting elements 1 to 4 including both the phosphorescent material and the fluorescent material as the material presenting the light emission have the same efficiency as the comparative light-emitting element 5 including only the fluorescent material as the material presenting the light emission. That is, by using the fluorescent material having the protective group as the light-emitting body, even if both the phosphorescent material and the fluorescent material are used as the material presenting the light emission, the light-emitting element with high light emission efficiency can be manufactured. In addition, the comparative light-emitting element 5 can be regarded as a light-emitting element having a phosphorescent material concentration of 0. Therefore, by adjusting one or both of the concentration of the fluorescent material having the protective group and the concentration of the phosphorescent material contributing to the light emission, the light emission color can be adjusted while maintaining high light emission efficiency. At this time, the concentration of the fluorescent material having a protecting group is preferably higher than that of the phosphorescent material because the luminescence of the fluorescent material and the luminescence of the phosphorescent material can be obtained in a balanced manner.

〈CV measurement results〉

Next, the electrochemical characteristics (oxidation reaction characteristics and reduction reaction characteristics) of 4,6mCzP2Pm and Ir(ppz) ₃ used in the light-emitting layer of each light-emitting element were measured by cyclic voltammetry (CV).

As a measuring instrument, an electrochemical analyzer (ALS Model 600A or 600C manufactured by BAS Inc.) was used. In addition, the solution used for CV measurement was prepared as follows: as a solvent, dehydrated dimethylformamide (DMF) (manufactured by Aldrich Corporation, 99.8%, catalog number: 22705-6) was used, tetra-n-butylammonium perchlorate (n-Bu ₄ NClO ₄ ) (manufactured by Tokyo Chemical Industry Co., Ltd., catalog number: T0836) as a supporting electrolyte was dissolved at a concentration of 100 mmol/L, and the measurement object was dissolved at a concentration of 2 mmol/L. In addition, a platinum electrode (made by BAS Inc., PTE platinum electrode) was used as the working electrode, a platinum electrode (made by BAS Inc., Pt counter electrode (5 cm) for VC-3) was used as the auxiliary electrode, and an Ag/Ag ⁺ electrode (made by BAS Inc., RE7 non-aqueous solvent reference electrode) was used as the reference electrode. In addition, the measurement was carried out at room temperature (20 to 25°C). The scanning speed during CV measurement was unified to 0.1 V/sec, and the oxidation potential Ea [V] and reduction potential Ec [V] relative to the reference electrode were measured. Ea is the middle potential between the oxidation-reduction wave, and Ec is the middle potential between the reduction-oxidation wave. Here, it is known that the potential energy of the reference electrode used in this embodiment relative to the vacuum energy level is -4.94 [eV], so the HOMO energy level [eV] = -4.94-Ea, LUMO energy level [eV] = -4.94-Ec are used to calculate the HOMO energy level and the LUMO energy level respectively.

According to the CV measurement results, the oxidation potential of 4,6mCzP2Pm is 0.95V, and the reduction potential is -2.06V. In addition, the HOMO energy level of 4,6mCzP2Pm calculated by CV measurement is -5.89eV, and the LUMO energy level is -2.88eV. In addition, the oxidation potential of Ir(ppz) ₃ is 0.45V, and the reduction potential is -3.17V. In addition, the HOMO energy level of Ir(ppz) ₃ calculated by CV measurement is -5.39eV, and the LUMO energy level is -1.77eV.

As described above, the LUMO energy level of 4,6mCzP2Pm is lower than that of Ir(ppz) ₃ , while the HOMO energy level of Ir(ppz) ₃ is higher than that of 4,6mCzP2Pm. Therefore, when the compound is used in the light-emitting layer, electrons and holes can be efficiently injected into 4,6mCzP2Pm and Ir(ppz) ₃ , respectively, so that 4,6mCzP2Pm and Ir(ppz) ₃ form an excited state complex. In addition, as shown in FIG16, the excited state complex formed by 4,6mCzP2Pm and Ir(ppz) ₃ has a light emission peak near 530nm.

As shown in Figure 16, the emission spectrum obtained from the excited complex formed by 4,6mCzP2Pm and Ir(ppz) ₃ overlaps with both the absorption spectrum of 2TMS-mmtBuDPhA2Anth and the absorption spectrum of It(dmdppr-dmp) ₂ (dpm). Therefore, the excitation energy possessed by the excited complex can be efficiently transferred to 2TMS-mmtBuDPhA2Anth and Ir(dmdppr-dmp) ₂ (dpm). In addition, the emission spectrum of 2TMS-mmtBuDPhA2Anth overlaps with the absorption spectrum of Ir(dmdppr-dmp) ₂ (dpm). Therefore, energy transfer from 2TMS-mmtBuDPhA2Anth to Ir(dmdppr-dmp) ₂ (dpm) can also occur. Therefore, by an implementation method of the present invention, a multi-color light-emitting element with good light-emitting efficiency can be manufactured.

Embodiment 2

In this embodiment, a light-emitting element of an embodiment of the present invention different from the above-mentioned embodiment and a manufacturing example of a comparative light-emitting element and the characteristics of the light-emitting element are described. The structure of the light-emitting element manufactured in this embodiment is the same as that of FIG. 1A. Tables 4 and 5 show the details of the element structure. The structures and abbreviations of the compounds used are shown below. For other organic compounds, reference can be made to the above-mentioned embodiment and the above-mentioned embodiment.

[Table 5]

<<Manufacturing of Light-Emitting Element 4, Light-Emitting Element 6, and Comparative Light-Emitting Element 7 to Comparative Light-Emitting Element 9>>

The element structure of the light-emitting element 4 is shown in Example 1 and Table 3. Similarly, the manufacturing process of the light-emitting element 6 and the comparative light-emitting elements 7 to 9 is different from that of the light-emitting element 1 only in the manufacturing process of the light-emitting layer 130, and the other processes are the same as the manufacturing method of the light-emitting element 1. The details of the element structure are shown in Table 3, so the details of the manufacturing method are omitted. The comparative light-emitting elements 7 and 8 are light-emitting elements using MeDPhA2A, a fluorescent material without a protective group, and the comparative light-emitting element 9 is a light-emitting element that does not contain a fluorescent material.

<Characteristics of Light Emitting Element>

Next, the device characteristics of the light-emitting element 4, the light-emitting element 6, and the comparative light-emitting element 7 to the comparative light-emitting element 9 manufactured as described above were measured. The measurement method was the same as that of the first embodiment.

Fig. 17 shows the external quantum efficiency-luminance characteristics of the light-emitting element 4, the light-emitting element 6, and the comparative light-emitting elements 7 to 9. Fig. 18 shows the electroluminescence spectra when a current of 2.5 mA/ ^cm2 is passed through the light-emitting element 4, the light-emitting element 6, and the comparative light-emitting element 7 to 9. The measurement of each light-emitting element was performed at room temperature (an atmosphere maintained at 23°C).

Table 6 shows the device characteristics of Light Emitting Element 4, Light Emitting Element 6, and Comparative Light Emitting Element 7 to Comparative Light Emitting Element 9 at around 1000 cd/m ² .

As shown in FIG. 18 , it can be seen that the emission spectra of light-emitting element 4 and light-emitting element 6 have two peaks near 530 nm and near 610 nm. The peak near 530 nm originates from 2TMS-mmtBuDPhA2Anth, and the peak near 610 nm originates from Ir(dmdppr-dmp) ₂ (dpm). In other words, it can be seen that both the light-emitting element 4 and light-emitting element 6 obtain the light-emitting element originating from 2TMS-mmtBuDPhA2Anth and the light-emitting element originating from Ir(dmdppr-dmp) ₂ (dpm). Similarly, it can be seen that the comparison light-emitting element 7 and comparison light-emitting element 8 have two peaks near 530 nm and near 610 nm. The peak near 530 nm originates from MeDPhA2A, and the peak near 610 nm originates from Ir(dmdppr-dmp) ₂ (dpm). That is, it can be seen that both the luminescence derived from MeDPhA2A and the luminescence derived from Ir(dmdppr-dmp) ₂ (dpm) are obtained in the comparative luminescent element 7 and the comparative luminescent element 8. In addition, green luminescence with a peak wavelength of 531 nm and a half width of 88 nm is obtained in the comparative luminescent element 9. Therefore, it can be seen that the luminescence derived from the excited state complex formed by 4,6mCzP2Pm and Ir(ppz) ₃ is obtained in the comparative luminescent element 9.

In addition, as shown in FIG. 17 , although the light-emitting element 4 and the light-emitting element 6 exhibit light emission derived from the fluorescent material, they have high external quantum efficiency equal to or higher than that of the comparative light-emitting element 9. On the other hand, the comparative light-emitting element 7 and the comparative light-emitting element 8 exhibit significantly lower external quantum efficiency than that of the comparative light-emitting element 9. The light-emitting element 4, the light-emitting element 6, the comparative light-emitting element 7, and the comparative light-emitting element 8 can be regarded as elements to which the fluorescent material and the phosphorescent material are added to the comparative light-emitting element 9. That is, although the light-emitting element 4 and the light-emitting element 6 have the fluorescent material added, multi-color light emission is obtained while maintaining the light emission efficiency equal to that of the comparative light-emitting element 9. On the other hand, in the comparative light-emitting element 7 and the comparative light-emitting element 8, the light emission efficiency is reduced due to the addition of the fluorescent material and the phosphorescent material. Since the light-emitting element 4, the light-emitting element 6, the comparative light-emitting element 7 and the comparative light-emitting element 8 use the same phosphorescent material, it can be said that the reason for the decrease in efficiency of the comparative light-emitting element 7 and the comparative light-emitting element 8 is the fluorescent material. It can be considered that the use of a fluorescent material without a protecting group leads to the deactivation of triplet excitons. On the other hand, in a light-emitting element of an embodiment of the present invention, the non-radiative deactivation of triplet excitons is suppressed, and it is efficiently converted into light emission. It can be seen that by using a fluorescent material with a protecting group in the light-emitting layer, the energy transfer based on the Dexter mechanism of triplet excitation energy from the host material and the phosphorescent material to the fluorescent material and the non-radiative deactivation of triplet excitation energy can be suppressed.

In addition, the concentration of the fluorescent material having a protecting group is different between the light-emitting element 4 and the light-emitting element 6. Similarly, the concentration of the fluorescent material having no protecting group is different between the comparative light-emitting element 7 and the comparative light-emitting element 8. Here, according to Table 4, the reduction ratio of the external quantum efficiency between the light-emitting element 4 and the light-emitting element 6 {(external quantum efficiency of the light-emitting element 4-external quantum efficiency of the light-emitting element 6)/external quantum efficiency of the light-emitting element 4×100} is about 15%, while the reduction ratio of the external quantum efficiency between the comparative light-emitting element 7 and the comparative light-emitting element 8 {(external quantum efficiency of the comparative light-emitting element 7-external quantum efficiency of the comparative light-emitting element 8)/external quantum efficiency of the comparative light-emitting element 7×100} is about 30%. Therefore, it can be seen that by using a fluorescent material having a protecting group, a decrease in efficiency due to an increase in the concentration of the fluorescent material can be suppressed.

<Brightness Change of Light Emitting Element>

FIG19 shows the chromaticity-brightness characteristics of the light-emitting element 4 and the light-emitting element 6. According to FIG19, it can be seen that the chromaticity x and the chromaticity y of the light-emitting element 4 and the light-emitting element 6 are almost unchanged according to the brightness. That is, the light-emitting element 4 and the light-emitting element 6 are light-emitting elements with stable luminous colors and very little color change due to brightness change. This is because the fluorescent material and the phosphorescent material in the light-emitting element 4 and the light-emitting element 6 generate light by energy transfer from the excitation energy of the energy donor. Therefore, it can be seen that: by an embodiment of the present invention, a light-emitting element that exhibits multi-color light emission with little color change due to brightness can be manufactured.

<Reliability test of light-emitting components>

Next, a 2 mA constant current driving test was performed on the light-emitting element 6, the comparative light-emitting element 5, and the comparative light-emitting element 9. The results are shown in FIG20. As can be seen from FIG20, compared with the driving life of the comparative light-emitting element 9 not including the fluorescent material and the phosphorescent material, the driving life of the comparative light-emitting element 5 including the fluorescent material is good, and the driving life of the light-emitting element 6 including the fluorescent material and the phosphorescent material is even better. That is, by an embodiment of the present invention, a light-emitting element that has high luminous efficiency and good reliability and exhibits multi-color luminescence can be manufactured.

Next, FIG. 21 shows the electroluminescence spectrum of the light-emitting element 6 whose brightness is reduced to 50% by the reliability test, and the electroluminescence spectrum of the light-emitting element 6 at 2.5 mA/ ^cm2 before the reliability test. The spectrum intensity shown in FIG. 21 is normalized for comparison of the spectrum shape. According to FIG. 21, it can be seen that the shape of the electroluminescence spectrum of the light-emitting element 6 is almost unchanged before and after the reliability test. This is because the fluorescent material and the phosphorescent material in the light-emitting element 6 generate light through energy transfer from the excitation energy of the energy donor. Therefore, it can be seen that: by an embodiment of the present invention, a light-emitting element that exhibits multi-color light emission with little color change before and after driving can be manufactured.

Embodiment 3

In this embodiment, a light-emitting element of an embodiment of the present invention different from the above-mentioned embodiment and a manufacturing example of a comparative light-emitting element and the characteristics of the light-emitting element are described. The structure of the light-emitting element manufactured in this embodiment is the same as that of FIG. 1A. Table 7 shows the details of the element structure. The structures and abbreviations of the compounds used are shown below. For other organic compounds, reference can be made to the above-mentioned embodiment and the above-mentioned embodiment.

[Compound 39]

《Manufacturing of Light-Emitting Element 10, Comparative Light-Emitting Element 11 and Comparative Light-Emitting Element 12》

The manufacturing process of the light-emitting element 10, the comparative light-emitting element 11 and the comparative light-emitting element 12 is different from that of the light-emitting element 1 only in the manufacturing process of the hole transport layer 112 and the light-emitting layer 130, and the other processes are the same as the manufacturing method of the light-emitting element 1. The details of the element structure are shown in Table 7, so the details of the manufacturing method are omitted. In the light-emitting element 10, light emission of the fluorescent material 1,3,8,10-tetra-tert-butyl-7,14-bis(3,5-di-tert-butylphenyl)-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione (abbreviated as: Oct-tBuDPQd) having a protective group and the phosphorescent material Ir(dmdppr-dm) ₂ (dpm) is obtained, and the details will be described later.

In addition, the light-emitting element 10 can be regarded as a light-emitting element in which a phosphorescent material is added to the comparative light-emitting element 11. In addition, the comparative light-emitting element 11 can be regarded as a light-emitting element in which a fluorescent material having a protective group is added to the comparative light-emitting element 12. Therefore, the light-emitting element 10 can be regarded as an element in which a fluorescent material having a protective group and a phosphorescent material are added to the comparative light-emitting element 12.

<Characteristics of Light Emitting Element>

Next, the device characteristics of the light-emitting device 10, the comparative light-emitting device 11, and the comparative light-emitting device 12 manufactured as described above were measured. The measurement method was the same as that of the first embodiment.

Fig. 26 shows the external quantum efficiency-luminance characteristics of the light-emitting element 10, the comparative light-emitting element 11, and the comparative light-emitting element 12. Fig. 27 shows the electroluminescence spectrum when a current of 2.5 mA/ ^cm2 is passed through the light-emitting element 10, the comparative light-emitting element 11, and the comparative light-emitting element 12. The measurement of each light-emitting element was performed at room temperature (an atmosphere maintained at 23°C).

Table 8 shows the device characteristics of the light-emitting element 10, the comparative light-emitting element 11, and the comparative light-emitting element 12 at around 1000 cd/m ² .

As shown in FIG27 , it can be seen that the emission spectrum of the light-emitting element 10 has two peaks near 526 nm and near 608 nm. The peak near 526 nm originates from Oct-tBuDPQd, and the peak near 608 nm originates from Ir(dmdppr-dmp) ₂ (dpm). In other words, it can be seen that both the light emission originating from Oct-tBuDPQd and the light emission originating from Ir(dmdppr-dmp) ₂ (dpm) are obtained in the light-emitting element 10. In addition, it can be seen that the comparison light-emitting element 11 has a peak near a wavelength of 526 nm. The peak near 526 nm originates from Oct-tBuDPQd. In addition, it can be seen that the emission spectrum of the comparison light-emitting element 12 has a peak near 506 nm, and its half-width is 81 nm. The light emission of the comparison light-emitting element 12 originates from 3Cz2DPhCzBN. Non-patent document 1 states that 3Cz2DPhCzBN is a TADF material.

In addition, as shown in FIG. 26 , although the light-emitting element 10 exhibits light emission from the fluorescent material, it has a high external quantum efficiency equal to or higher than that of the comparative light-emitting element 12. In addition, the light-emitting element 10 has a higher external quantum efficiency than that of the comparative light-emitting element 11. Therefore, in the light-emitting element 10, light emission from both the fluorescent material and the phosphorescent material is obtained, and a higher light emission efficiency is obtained than that of the comparative light-emitting element 11 and the comparative light-emitting element 12. As described above, this is because the non-radiative deactivation of triplet excitons is suppressed in the light-emitting element of one embodiment of the present invention, and it is efficiently converted into light emission.

In addition, in the light-emitting element 10, a TADF material is used as an energy donor. Therefore, the TADF material is suitable for use in the light-emitting element of an embodiment of the present invention. In addition, in the light-emitting element 10, an organic compound containing a quinacridone skeleton in the light-emitting body is used as a fluorescent material having a protective group. Therefore, an organic compound containing a quinacridone skeleton is suitable for use in the light-emitting element of an embodiment of the present invention.

Embodiment 4

In this embodiment, a light-emitting element of an embodiment of the present invention different from the above-mentioned embodiment and a manufacturing example of a comparative light-emitting element and the characteristics of the light-emitting element are described. The structure of the light-emitting element manufactured in this embodiment is the same as that of FIG. 1A. Table 7 shows the details of the element structure. The structures and abbreviations of the compounds used are shown below. For other organic compounds, reference can be made to the above-mentioned embodiment and the above-mentioned embodiment.

《Manufacturing of light-emitting element 13》

The manufacturing process of the light emitting element 13 is different from that of the light emitting element 10 described above only in the manufacturing process of the light emitting layer 130, and the other processes are the same as the manufacturing method of the light emitting element 10. The details of the element structure are shown in Table 9, so the details of the manufacturing method are omitted.

<Characteristics of Light Emitting Element>

Next, the device characteristics of the light emitting device 13 manufactured as described above are measured. The measurement method is the same as that of the first embodiment.

Fig. 28 shows the external quantum efficiency-luminance characteristics of the light-emitting element 13. Fig. 29 shows the electroluminescence spectrum when a current of 2.5 mA/cm ² is passed through the light-emitting element 13. The light-emitting element was measured at room temperature (an atmosphere maintained at 23°C).

In addition, Table 10 shows the device characteristics of the light-emitting device 13 near 3 cd/m ² .

As shown in FIG. 29 , it can be seen that the emission spectrum of the light-emitting element 13 has two peaks near 527 nm and near 567 nm. The peak near 527 nm originates from Oct-tBuDPQd, and the peak near 567 nm originates from 7,10-bis(4-(diphenylamino)phenyl)-2,3-dicyanopyrazinephenanthrene (abbreviated as: TPA-DCPP) which is a TADF material. In other words, it can be seen that both the light emission originating from Oct-tBuDPQd and the light emission originating from TPA-DCPP are obtained in the light-emitting element 13. Non-patent document 2 states that TPA-DCPP is a TADF material.

In addition, as shown in FIG. 28 , although the light-emitting element 13 exhibits light emission derived from the fluorescent material, a high external quantum efficiency exceeding the theoretical efficiency of a general fluorescent element is obtained.

Reference Example 1

In this reference example, a method for synthesizing 2TMS-mmtBuDPhA2Anth (structural formula (229)) which is a fluorescent material having a protective group and is used in Examples 1 and 2 is described.

<Step 1: Synthesis of 9,10-dibromo-2-trimethylsilanthracene>

2.7 g (11 mmol) of 2-trimethylsilanthracene was placed in a 500 mL three-necked flask, and the air in the flask was replaced with nitrogen. 110 mL of N,N-dimethylsulfoxide was added, and the mixture was stirred at room temperature. 4.0 g (23 mmol) of N-bromosuccinimide was added, and the mixture was stirred at room temperature for 15 hours. After stirring, water was added to the reaction mixture to obtain an aqueous layer and an organic layer. The aqueous layer was extracted with toluene, and the obtained extract and organic layer were combined. The mixed solution of the extract and the organic layer was washed with water and a saturated sodium thiosulfate aqueous solution, and then dried with magnesium sulfate. The mixture was separated by gravity filtration, and the filtrate was concentrated to obtain a yellow-brown solid. After adding 450 mL of hexane and 50 mL of toluene to the obtained yellow-brown solid, it was suction filtered by magnesium silicate (Wako Pure Chemical Industries, Ltd., catalog number: 066-05265), diatomaceous earth (Wako Pure Chemical Industries, Ltd., catalog number: 537-02305) and alum to obtain a filtrate. The obtained filtrate was concentrated to obtain a yellow-brown solid. The obtained solid was recrystallized using ethyl acetate/ethanol to obtain 2.4 g of a yellow solid with a yield of 54%. The synthesis scheme (F-1) of step 1 is shown below.

[Chemical formula 41]

In addition, the measurement results of the yellow solid obtained by the above step 1 using ¹ H NMR are shown below. In addition, FIG. 22A, FIG. 22B, and FIG. 23 show ¹ H NMR spectra. FIG. 22B is an enlarged view of the range of 6.5 ppm to 9.0 ppm of FIG. 22A. In addition, FIG. 23 is an enlarged view of the range of 0.0 ppm to 2.0 ppm of FIG. 22A. From this result, it can be seen that 9,10-dibromo-2-trimethylsilanthracene is obtained.

¹ H NMR (CDCl ₃ ,300MHz): σ=8.74(s,1H), 8.63-8.56(m,2H), 8.55(d,J=8.8Hz,1H), 7.75(d,J=8.3Hz,1H ), 7.68-7.61(m,2H), 0.42(s,9H).

<Step 2: Synthesis of 2TMS-mmtBuDPhA2Anth>

1.4 g (3.3 mmol) of 9,10-dibromo-2-trimethylsilanthracene, 2.6 g (6.6 mmol) of bis(3,5-tert-butylphenyl)amine, 1.3 g (14 mmol) of sodium tert-butoxide, and 60 mg (0.15 mmol) of 2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl (abbreviated as: SPhos) were placed in a 200 mL three-necked flask, and the air in the flask was replaced with nitrogen. 33 mL of xylene was added to the mixture, and the mixture was degassed under reduced pressure. 40 mg (70 μmol) of bis(dibenzylideneacetone)palladium(0) was added to the mixture, and then the mixture was stirred at 150°C for 6 hours under a nitrogen flow. After stirring, 400 mL of toluene was added to the obtained mixture, and then the filtrate was obtained by suction filtration using magnesium silicate, diatomaceous earth, and alum. The obtained filtrate was concentrated to obtain a brown solid. The solid was purified by silica gel column chromatography (developing solvent: hexane: toluene = 9:1) to obtain a yellow solid. The obtained yellow solid was recrystallized using ethyl acetate and ethanol to obtain 0.40 g of the target yellow solid with a yield of 12%. The synthesis scheme of step 2 (F-2) is shown below.

[Chemical formula 42]

0.40 g of the obtained yellow solid was purified by gradient sublimation. The yellow solid was heated at 260° C. for 15 hours under a pressure of 3.5 Pa for sublimation purification. After sublimation purification, 0.35 g of the target yellow solid was obtained with a yield of 87%.

In addition, the measurement results of the yellow solid obtained by the above step 2 using ¹ H NMR are shown below. In addition, FIG. 24A, FIG. 24B, and FIG. 25 show ¹ H NMR spectra. FIG. 24B is an enlarged view of the range of 6.5 ppm to 9.0 ppm of FIG. 24A. In addition, FIG. 25 is an enlarged view of the range of 0.0 ppm to 2.0 ppm of FIG. 24A. From this result, it can be seen that 2TMS-mmtBuDPhA2Anth was obtained.

¹ H NMR (CDCl ₃ , 300MHz): σ=8.25(s,1H), 8.24-8.21(m,1H), 8.15-8.11(m,2H), 7.40-7.37(m,1H), 7.30-7.27( m,2H), 6.97-6.94(m,8H), 6.92-6.91(m,4H), 1.14(s,36H), 1.12(m,36H), 0.09(s,9H).

Reference Example 2

In this reference example, a method for synthesizing Oct-tBuDPQd (structural formula (104)) which is a fluorescent material having a protective group and is used in Examples 3 and 4 is described.

<Step 1: Synthesis of 1,4-cyclohexadiene-1,4-dicarboxylic acid, 2,5-bis{(3,5-di-tert-butylphenyl)amino}-dimethyl ester>

5.6 g (24 mmol) of 1,4-cyclohexanedione-2,5-dicarboxylic acid dimethyl and 10 g (48 mmol) of 3,5-di-tert-butylaniline were placed in a 200 mL three-necked flask equipped with a reflux tube, and the mixture was stirred at 170°C for 2 hours. Methanol was added to the obtained red-orange solid to make it slurry, and the mixture was collected by suction filtration. The obtained solid was washed with hexane and methanol, and dried to obtain 12 g of the target red-orange solid with a yield of 82%. The synthesis scheme (E-1) of step 1 is shown below.

The ¹ H NMR numerical data of the obtained solid are shown below. It can be seen from this that the target compound was obtained.

¹ H NMR (chloroform-d, 500 MHz): δ=10.6 (s, 2H), 7.20 (t, J=1.5 Hz, 2H), 6.94 (d, J=2.0 Hz, 4H), 3.65 (s, 6H), 3.48 (s, 4H), 1.33 (s, 36H).

<Step 2: Synthesis of 1,4-benzenedicarboxylic acid, 2,5-bis{(3,5-di-tert-butylphenyl)amino}-dimethyl ester>

12 g (20 mmol) of 1,4-cyclohexadiene-1,4-dicarboxylic acid, 2,5-bis{(3,5-di-tert-butylphenyl)amino}-dimethyl ester obtained in step 1 and 150 mL of toluene were placed in a 300 mL three-necked flask equipped with a reflux tube. While blowing air into the mixture, reflux was performed for 15 hours. After stirring, the precipitated solid was collected by suction filtration, and the obtained solid was washed with hexane and methanol to obtain 7.3 g of the target red solid. The obtained filtrate was concentrated to obtain a solid. The solid was washed with hexane and methanol, and the solid was collected by suction filtration to obtain 3.1 g of the target red solid. Thus, a total of 10.4 g of the target compound was obtained with a yield of 85%. The synthesis scheme (E-2) of step 2 is shown below.

The ¹ H NMR numerical data of the obtained solid are shown below. It can be seen from this that the target compound was obtained.

¹ H NMR (chloroform-d, 500MHz): δ=8.84(s,2H), 8.18(s,2H), 7.08(d,J=2.0Hz,4H), 7.20(t,J=1.0Hz,2H) , 3.83(s,6H), 1.34(s,36H).

<Step 3: Synthesis of 1,4-benzenedicarboxylic acid, 2,5-bis[N,N'-bis(3,5-di-tert-butylphenyl)amino]-dimethyl ester>

4.0 g (6.7 mmol) of 1,4-benzenedicarboxylic acid, 2,5-bis{(3,5-di-tert-butylphenyl)amino}-dimethyl ester obtained in step 2, 3.9 g (14.6 mmol) of 1-bromo-3,5-di-tert-butylbenzene, 0.46 g (7.3 mmol) of copper, 50 mg of copper iodide (0.26 mmol), 1.0 g (7.3 mmol) of potassium carbonate and 10 mL of xylene were placed in a 200 mL three-necked flask equipped with a reflux tube, the mixture was degassed under reduced pressure, and then the air in the system was replaced with nitrogen. The mixture was refluxed for 20 hours. 0.46 g (7.3 mmol) of copper and 50 mg of copper iodide (0.26 mmol) were added to the obtained mixture, and reflux was further performed for 16 hours. Dichloromethane was added to the obtained mixture to make it slurry. The solid was removed by suction filtration, and the obtained filtrate was concentrated. The obtained solid was washed with hexane and ethanol. The obtained solid was recrystallized with hexane/toluene to obtain 4.4 g of the target compound as a yellow solid with a yield of 72%. The synthesis scheme (E-3) of step 3 is shown below.

[Chemical formula 45]

The ¹ H NMR numerical data of the obtained solid are shown below. It can be seen from this that the target compound was obtained.

¹ H NMR (chloroform-d, 500MHz): δ=7.48 (s, 2H), 6.97 (t, J=2.0Hz, 4H), 7.08 (d, J=1.5Hz, 8H), 3.25 (s, 6H) ,1.23(s,72H).

<Step 4: Synthesis of 1,3,8,10-tetra-tert-butyl-7,14-bis(3,5-di-tert-butylphenyl)-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione (abbreviated as: Oct-tBuDPQd)>

4.4 g (4.8 mmol) of 1,4-benzenedicarboxylic acid, 2,5-bis[N,N'-bis(3,5-di-tert-butylphenyl)amino]-dimethyl ester obtained in step 3 and 20 mL of methanesulfonic acid were placed in a 100 mL three-necked flask equipped with a reflux tube, and the mixture was stirred at 160°C for 7 hours. After the mixture was cooled to room temperature, it was slowly added dropwise to 300 mL of ice water, and then left until the temperature reached room temperature. The above mixture was gravity filtered, and the obtained solid was washed with water and saturated sodium bicarbonate aqueous solution. The solid was dissolved in toluene, and the obtained toluene solution was washed with water and saturated brine, and dried with magnesium sulfate. The mixture was filtered through diatomaceous earth (Wako Pure Chemical Industries, Ltd., catalog number: 537-02305) and alum. The filtrate obtained was concentrated to obtain 3.3 g of a dark brown solid. The obtained solid was purified by silica gel column chromatography (developing solvent: hexane: ethyl acetate = 20:1) to obtain 150 mg of the target compound as a red-orange solid with a yield of 5%. The synthesis scheme of step 4 (E-4) is shown below.

In addition, the measurement results of the yellow solid obtained by the above step 4 using ¹ H NMR are shown below. In addition, FIG. 30A, FIG. 30B, and FIG. 31 show ¹ H NMR spectra. FIG. 30B is an enlarged view of the range of 6.5 ppm to 9.0 ppm of FIG. 30A. In addition, FIG. 31 is an enlarged view of the range of 0.5 ppm to 2.0 ppm of FIG. 30A. From this result, it can be seen that Oct-tBuDPQd was obtained.

¹ H NMR (chloroform-d, 500MHz): δ=8.00(s,2H), 7.65(t,J=2.0Hz,2H), 7.39(d,J=1.0Hz,4H), 7.20(d,J= 2.0Hz,2H), 6.50(d,J=1.0Hz,2H), 1.60(s,18H), 1.39(s,36H), 1.13(s,18H).

131‧‧‧Compound

132‧‧‧Compound

136‧‧‧Compound

Claims (24)

A light-emitting element comprises: a pair of electrodes; and a light-emitting layer between the pair of electrodes, wherein the light-emitting layer comprises a first material capable of converting triplet excitation energy into luminescence, a second material capable of converting singlet excitation energy into luminescence, and a third material capable of converting triplet excitation energy into luminescence, the second material comprises a luminophore and five or more protective groups, the luminophore is a fused aromatic ring or a fused heteroaromatic ring, the five or more protective groups independently have any one of an alkyl group having 1 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms, the lowest triplet excitation energy level of the first material is higher than the lowest triplet excitation energy level of the third material, and luminescence is obtained from both the second material and the third material. According to the light-emitting element of claim 1, at least four of the five protecting groups are independently any one of an alkyl group with 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group with 3 to 10 carbon atoms, and a trialkylsilyl group with 3 to 12 carbon atoms. A light-emitting element comprises: a pair of electrodes; and a light-emitting layer between the pair of electrodes, wherein the light-emitting layer comprises a first material capable of converting triplet excitation energy into light-emitting, a second material capable of converting singlet excitation energy into light-emitting, and a third material capable of converting triplet excitation energy into light-emitting, the second material comprises a light-emitting body and four or more protecting groups, the light-emitting body is a fused aromatic ring or a fused heteroaromatic ring, and the four or more protecting groups are not attached to the light-emitting body. The fused aromatic ring or the fused heteroaromatic ring is directly bonded, the four or more protecting groups independently include any one of an alkyl group with 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group with 3 to 10 carbon atoms, and a trialkylsilyl group with 3 to 12 carbon atoms, the lowest triplet excitation energy level of the first material is higher than the lowest triplet excitation energy level of the third material, and luminescence is obtained from both the second material and the third material. According to the light-emitting element of item 3 of the patent application, each of the four or more protecting groups is bonded to the light-emitting body through at least one amino group. A light-emitting element comprises: a pair of electrodes; and a light-emitting layer between the pair of electrodes, wherein the light-emitting layer comprises a first material capable of converting triplet excitation energy into light-emitting, a second material capable of converting singlet excitation energy into light-emitting, and a third material capable of converting triplet excitation energy into light-emitting, the second material comprises a light-emitting body and two or more diarylamine groups, the light-emitting body is a fused aromatic ring or a fused heteroaromatic ring, the two or more diarylamine groups are in a fused aromatic ring or a fused heteroaromatic ring, The invention relates to a heteroaromatic ring bond, wherein the aryl groups in the two or more diarylamine groups independently have at least one protecting group, and the protecting group independently has any one of an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms, the lowest triplet excitation energy level of the first material is higher than the lowest triplet excitation energy level of the third material, and luminescence is obtained from both the second material and the third material. A light-emitting element comprises: a pair of electrodes; and a light-emitting layer between the pair of electrodes, wherein the light-emitting layer comprises a first material capable of converting triplet excitation energy into light-emitting, a second material capable of converting singlet excitation energy into light-emitting, and a third material capable of converting triplet excitation energy into light-emitting, the second material comprises a light-emitting body and two or more diarylamine groups, the light-emitting body is a fused aromatic ring or a fused heteroaromatic ring, the two or more diarylamine groups are in a state of being ... Aromatic ring bonding, the aromatic groups in the two or more diarylamine groups independently have at least two protecting groups, and the protecting groups independently have any one of an alkyl group with 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group with 3 to 10 carbon atoms, and a trialkylsilyl group with 3 to 12 carbon atoms, the lowest triplet excitation energy level of the first material is higher than the lowest triplet excitation energy level of the third material, and luminescence is obtained from both the second material and the third material. A light-emitting element according to any one of claims 2 to 6, wherein the alkyl group is a branched alkyl group. A light-emitting element comprises: a pair of electrodes; and a light-emitting layer between the pair of electrodes, wherein the light-emitting layer comprises a first material capable of converting triplet excitation energy into light-emitting, a second material capable of converting singlet excitation energy into light-emitting, and a third material capable of converting triplet excitation energy into light-emitting, the second material comprises a light-emitting body and a plurality of protecting groups, the light-emitting body is a fused aromatic ring or a fused heteroaromatic ring, the plurality of protecting groups are At least one of the atoms of the protecting group is located directly above one face of the fused aromatic ring or the fused heteroaromatic ring, and at least one of the other atoms of the plurality of protecting groups is located directly above another face of the fused aromatic ring or the fused heteroaromatic ring, the lowest triplet excitation energy level of the first material is higher than the lowest triplet excitation energy level of the third material, and luminescence is obtained from both the second material and the third material. A light-emitting element comprises: a pair of electrodes; and a light-emitting layer between the pair of electrodes, wherein the light-emitting layer comprises a first material capable of converting triplet excitation energy into light-emitting, a second material capable of converting singlet excitation energy into light-emitting, and a third material capable of converting triplet excitation energy into light-emitting, the second material comprises a light-emitting body and two or more diphenylamine groups, the light-emitting body is a fused aromatic ring or a fused heteroaromatic ring, the two or more diphenylamine groups are in a fused aromatic ring or a fused heteroaromatic ring. Cyclic bonding, The phenyl groups in the two or more diphenylamine groups independently have protective groups at the 3-position and the 5-position, and the protective groups independently have any one of an alkyl group having 3 to 10 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms, and a trialkylsilyl group having 3 to 12 carbon atoms, the lowest triplet excitation energy level of the first material is higher than the lowest triplet excitation energy level of the third material, and luminescence is obtained from both the second material and the third material. According to the light-emitting element of item 9 of the patent application, the alkyl group is a branched alkyl group. According to the light-emitting element of item 10 of the patent application, the branched alkyl group contains a quaternary carbon. According to any one of claims 1 to 6, 8 and 9, the condensed aromatic ring or the condensed heteroaromatic ring comprises naphthalene, anthracene, fluorene,

, triphenylmethane, tetraphenylmethane, pyrene, perylene, coumarin, quinacridone and naphthodibenzofuran. A light-emitting element according to any one of claims 1 to 6, 8 and 9, wherein the first material comprises a first organic compound and a second organic compound, and the first organic compound and the second organic compound are capable of forming an excited complex with each other. According to the light-emitting element of item 13 of the patent application, the first organic compound is a phosphorescent compound. A light-emitting element according to any one of claims 1 to 6, 8 and 9, wherein the peak of the emission spectrum of the first material has a shorter wavelength than the peak of the emission spectrum of the second material. A light-emitting element according to any one of the patent application scopes 1 to 6, 8 and 9, wherein the first material is a phosphorescent compound. A light-emitting element according to any one of claims 1 to 6, 8 and 9, wherein the first material is a compound that emits delayed fluorescence. A light-emitting element according to any one of claims 1 to 6, 8 and 9, wherein the emission spectrum of the first material overlaps with the absorption band with the longest wavelength of the absorption spectrum of the second material. A light-emitting element according to any one of the patent application scopes 1 to 6, 8 and 9, wherein in the light-emitting layer, the concentration of the second material is higher than the concentration of the third material. A light-emitting element according to any one of the patent application scopes 1 to 6, 8 and 9, wherein the third material is a phosphorescent compound. A light-emitting element according to any one of claims 1 to 6, 8 and 9, wherein the peak of the emission spectrum of the second material has a shorter wavelength than the peak of the emission spectrum of the third material. A light-emitting device, comprising: a light-emitting element of any one of the patent application ranges 1 to 6, 8 and 9; and at least one of a color filter and a transistor. An electronic device, comprising: a light-emitting device as defined in claim 22; and at least one of a housing and a display unit. A lighting device, comprising: a light-emitting element of any one of the patent application scopes 1 to 6, 8 and 9; and a housing.

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